Allele Registry

Canonical Allele Identifier: PA099612

Gene: TTR HGNC NCBI

ClinVar RCV:

RCV000159436

RCV001228889

ClinVar Variation:

181702

HGVS (amino-acid)	Matching Registered Transcripts
NP_000362.1:p.Ala65Asp	CA297540 NM_000371.3:c.194C>A