Allele Registry

Canonical Allele Identifier: PA2825102556

Gene: MET HGNC NCBI

ClinVar RCV:

RCV000203960

RCV000562884

RCV003401108

ClinVar Variation:

220389

HGVS (amino-acid)	Matching Registered Transcripts
NP_000236.2:p.Val427Ile	CA348239 NM_000245.4:c.1279G>A