Allele Registry

Canonical Allele Identifier: PA916027587

Gene: MET HGNC NCBI

ClinVar RCV:

RCV000153492

RCV001850098

RCV002354358

ClinVar Variation:

167293

HGVS (amino-acid)	Matching Registered Transcripts
NP_001311331.1:p.Gly840Ser	CA234266 NM_001324402.2:c.2518G>A