Allele Registry

Canonical Allele Identifier: PA2580217099

Gene: MET HGNC NCBI

ClinVar RCV:

RCV002963055

ClinVar Variation:

2074806

HGVS (amino-acid)	Matching Registered Transcripts
NP_001311331.1:p.Val841Glu	CA369117748 NM_001324402.2:c.2522T>A