Allele Registry

Canonical Allele Identifier: PA2825104281

Gene: MET HGNC NCBI

ClinVar RCV:

RCV000628769

RCV000765921

RCV001021839

RCV001766335

RCV002268220

RCV003459489

ClinVar Variation:

524889

HGVS (amino-acid)	Matching Registered Transcripts
NP_000236.2:p.Ile1345Thr	CA4448820 NM_000245.4:c.4034T>C