Allele Registry

Canonical Allele Identifier: PA100174

Gene: TTR HGNC NCBI

ClinVar RCV:

RCV000223926

RCV003514317

ClinVar Variation:

181700

HGVS (amino-acid)	Matching Registered Transcripts
NP_000362.1:p.Tyr136Ser	CA297535 NM_000371.3:c.407A>C