Allele Registry

Canonical Allele Identifier: PA916027576

Gene: MET HGNC NCBI

ClinVar RCV:

RCV000437499

ClinVar Variation:

376728

HGVS (amino-acid)	Matching Registered Transcripts
NP_001311331.1:p.Asp798His	CA16603136 NM_001324402.2:c.2392G>C