Allele Registry

Canonical Allele Identifier: PA100258

Gene: TTR HGNC NCBI

ClinVar RCV:

RCV000014382

RCV001173291

RCV002390107

RCV003050501

ClinVar Variation:

13440

2138144

HGVS (amino-acid)	Matching Registered Transcripts
NP_000362.1:p.Val50Leu	CA256825 NM_000371.3:c.148G>C CA402156746 NM_000371.3:c.148G>T