Allele Registry

Canonical Allele Identifier: PA2825101898

Gene: MET HGNC NCBI

ClinVar RCV:

RCV000628754

RCV002269292

RCV002334046

ClinVar Variation:

524875

HGVS (amino-acid)	Matching Registered Transcripts
NP_000236.2:p.Ile116Val	CA368968875 NM_000245.4:c.346A>G