Allele Registry

Canonical Allele Identifier: PA2580217078

Gene: MET HGNC NCBI

ClinVar RCV:

RCV002627583

ClinVar Variation:

1937117

HGVS (amino-acid)	Matching Registered Transcripts
NP_001311331.1:p.Lys763Arg	CA368991057 NM_001324402.2:c.2288A>G