Allele Registry

Canonical Allele Identifier: PA2580217050

Gene: MET HGNC NCBI

ClinVar RCV:

RCV002268845

ClinVar Variation:

1697561

HGVS (amino-acid)	Matching Registered Transcripts
NP_001311331.1:p.His664Pro	CA164908384 NM_001324402.2:c.1991A>C