Allele Registry

Canonical Allele Identifier: PA916027205

Gene: MET HGNC NCBI

ClinVar RCV:

RCV000628754

RCV002269292

RCV002334046

ClinVar Variation:

524875

HGVS (amino-acid)	Matching Registered Transcripts
NP_001311330.1:p.Ile116Val	CA368968875 NM_001324401.3:c.346A>G