Allele Registry

Canonical Allele Identifier: PA2827253843

Gene: MET HGNC NCBI

ClinVar Allele:

474469

ClinVar RCV:

RCV000567437

RCV000821666

RCV001293997

ClinVar Variation:

485767

HGVS (amino-acid)	Matching Registered Transcripts
NP_001311331.1:p.Ser118Leu	CA4448215 NM_001324402.2:c.353C>T