Canonical Allele Identifier: PA2825102377
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 132694

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000236.2:p.Ala347Thr
CA160433
NM_000245.4:c.1039G>A