Allele Registry

Canonical Allele Identifier: PA2825621677

Gene: MET HGNC NCBI

ClinVar RCV:

RCV003037254

ClinVar Variation:

2136594

HGVS (amino-acid)	Matching Registered Transcripts
NP_001120972.1:p.Val1110Leu	CA368989570 NM_001127500.3:c.3328G>C CA368989572 NM_001127500.3:c.3328G>T