Allele Registry

Canonical Allele Identifier: PA2580217049

Gene: MET HGNC NCBI

ClinVar RCV:

RCV003037254

ClinVar Variation:

2136594

HGVS (amino-acid)	Matching Registered Transcripts
NP_001311331.1:p.Val662Leu	CA368989570 NM_001324402.2:c.1984G>C CA368989572 NM_001324402.2:c.1984G>T