Allele Registry

Canonical Allele Identifier: PA2827253686

Gene: MET HGNC NCBI

ClinVar RCV:

RCV001324775

ClinVar Variation:

1024574

HGVS (amino-acid)	Matching Registered Transcripts
NP_001311331.1:p.Ser11Cys	CA368972928 NM_001324402.2:c.32C>G