Allele Registry

Canonical Allele Identifier: PA916027581

Gene: MET HGNC NCBI

ClinVar RCV:

RCV000437665

RCV000443188

ClinVar Variation:

376200

HGVS (amino-acid)	Matching Registered Transcripts
NP_001311331.1:p.Tyr805Asp	CA16602655 NM_001324402.2:c.2413T>G