Allele Registry

Canonical Allele Identifier: PA2825618869

Gene: MET HGNC NCBI

ClinVar RCV:

RCV001061413

RCV002235116

RCV002427037

RCV003046777

ClinVar Variation:

661481

856034

2122261

HGVS (amino-acid)	Matching Registered Transcripts
NP_001120972.1:p.Met362Ile	CA4448066 NM_001127500.3:c.1086G>C CA4448067 NM_001127500.3:c.1086G>A CA368970503 NM_001127500.3:c.1086G>T