Allele Registry

Canonical Allele Identifier: PA100014

Gene: TTR HGNC NCBI

ClinVar RCV:

RCV000014403

RCV002408461

ClinVar Variation:

13461

HGVS (amino-acid)	Matching Registered Transcripts
NP_000362.1:p.Phe64Ser	CA123116 NM_000371.3:c.191T>C