Canonical Allele Identifier: PA916027310
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 132694

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311330.1:p.Ala347Thr
CA160433
NM_001324401.3:c.1039G>A