Allele Registry

Canonical Allele Identifier: PA658669437

Gene: MET HGNC NCBI

ClinVar RCV:

RCV000541456

RCV001016448

RCV001591188

RCV002476079

RCV003392361

RCV003444568

ClinVar Variation:

454219

HGVS (amino-acid)	Matching Registered Transcripts
NP_001120972.1:p.Thr913Met	CA4448549 NM_001127500.3:c.2738C>T