Allele Registry

Canonical Allele Identifier: PA916027250

Gene: MET HGNC NCBI

ClinVar RCV:

RCV000034533

RCV000163435

RCV000485340

RCV001081506

RCV001252075

RCV001333795

ClinVar Variation:

41628

HGVS (amino-acid)	Matching Registered Transcripts
NP_001311330.1:p.Ser203Thr	CA188271 NM_001324401.3:c.607T>A