Canonical Allele Identifier: PA2827254032
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 411891
ClinVar Variation Id: 1782924
ClinVar RCV Id: RCV002410957

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311331.1:p.Gly215Arg
CA4448325
NM_001324402.2:c.643G>A
CA368979437
NM_001324402.2:c.643G>C