Allele Registry

Canonical Allele Identifier: PA100272

Gene: TTR HGNC NCBI

ClinVar RCV:

RCV000014359

RCV000159423

RCV000770555

RCV001173292

RCV002390106

RCV002476964

RCV004549361

ClinVar Variation:

13417

HGVS (amino-acid)	Matching Registered Transcripts
NP_000362.1:p.Val50Met	CA256790 NM_000371.3:c.148G>A