Allele Registry

Canonical Allele Identifier: PA2825103854

Gene: MET HGNC NCBI

ClinVar RCV:

RCV003037254

ClinVar Variation:

2136594

HGVS (amino-acid)	Matching Registered Transcripts
NP_000236.2:p.Val1092Leu	CA368989570 NM_000245.4:c.3274G>C CA368989572 NM_000245.4:c.3274G>T