AmbryLink is Ambry's comprehensive patient testing program that provides the confidence to identify rare-disease patients quickly and accurately.
Offering anonymous, no-cost genetic testing and confidential genetic counseling to patients suspected of having or clinically diagnosed with hATTR amyloidosis through the hATTR Compass program.
Choose an option below to order your kit and start your genetic testing.
Offering no-cost, confidential genetic testing program for patients who have a clinical history involving congenital hypotonia and specific types of movement disorders. This includes disorders such as aromatic L-amino acid decarboxylase (AADC) deficiency, several types of dystonias and dyskinesias, and other clinically overlapping conditions.
Learn MoreThis program offers no-cost, confidential genetic testing for patients who have a clinical history of severe hypertriglyceridemia. The panel tests for underlying genetic causes like Familial Chylomicronemia Syndrome (FCS) and hyperlipoproteinemia.
Choose an option below to order your kit and start your genetic testing.