Canonical Allele Identifier: PA2825103266
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 645086

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000236.2:p.Thr787Ala
CA368982573
NM_000245.4:c.2359A>G