Canonical Allele Identifier: PA2827253408
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 645086

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311330.1:p.Thr787Ala
CA368982573
NM_001324401.3:c.2359A>G