Allele Registry

Canonical Allele Identifier: PA123108

Gene: TTR HGNC NCBI

ClinVar RCV:

RCV000014394

RCV000036379

RCV000250966

RCV001127884

RCV001173541

RCV001711070

RCV002496358

RCV003125830

ClinVar Variation:

13452

HGVS (amino-acid)	Matching Registered Transcripts
NP_000362.1:p.Gly26Ser	CA123106 NM_000371.3:c.76G>A