Canonical Allele Identifier: PA2827253367
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 1061371

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311330.1:p.Gly762Asp
CA368982027
NM_001324401.3:c.2285G>A