Description: Mutations in Hereditary Amyloidosis
ttr (49) afib (13) fga (10) attr (6) fibrinogen (3) transthyretin (2) mutations in hereditary amyloidosis (1) apolipoprotein (1) apolipoprotein a1 (1) apolipoprotein a2 (1)
An online database for Hereditary Amyloidosis. The registry of Mutations in Hereditary Amyloidosis is edited by Dr. Dorota Rowczenio and Dr. Ashu Wechalekar, National Amyloidosis Centre, London, UK. Please use the forms to submit the mutations. All mutations are described according to recommendations of Human Genome Variation Society (HGVS) - www.hgvs.org/rec.html.
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