Allele Registry

Canonical Allele Identifier: PA099912

Gene: TTR HGNC NCBI

ClinVar RCV:

RCV000014366

RCV003162251

ClinVar Variation:

13424

HGVS (amino-acid)	Matching Registered Transcripts
NP_000362.1:p.Leu131Met	CA256804 NM_000371.3:c.391C>A