Allele Registry

Canonical Allele Identifier: PA2827253717

Gene: MET HGNC NCBI

ClinVar RCV:

RCV001237256

ClinVar Variation:

963255

HGVS (amino-acid)	Matching Registered Transcripts
NP_001311331.1:p.Gly26Arg	CA368973062 NM_001324402.2:c.76G>A CA368973064 NM_001324402.2:c.76G>C