Allele Registry

Canonical Allele Identifier: PA916027565

Gene: MET HGNC NCBI

ClinVar RCV:

RCV002234389

ClinVar Variation:

524887

HGVS (amino-acid)	Matching Registered Transcripts
NP_001311331.1:p.Val758Ile	CA4448748 NM_001324402.2:c.2272G>A