Allele Registry

Canonical Allele Identifier: PA2825103499

Gene: MET HGNC NCBI

ClinVar RCV:

RCV000541456

RCV001016448

RCV001591188

RCV002476079

RCV003392361

RCV003444568

ClinVar Variation:

454219

HGVS (amino-acid)	Matching Registered Transcripts
NP_000236.2:p.Thr895Met	CA4448549 NM_000245.4:c.2684C>T