Allele Registry

Canonical Allele Identifier: PA2825103857

Gene: MET HGNC NCBI

ClinVar RCV:

RCV002268845

ClinVar Variation:

1697561

HGVS (amino-acid)	Matching Registered Transcripts
NP_000236.2:p.His1094Pro	CA164908384 NM_000245.4:c.3281A>C