Canonical Allele Identifier: PA2825103222
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 1061371

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000236.2:p.Gly762Asp
CA368982027
NM_000245.4:c.2285G>A