Canonical Allele Identifier: PA915966568
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 411908

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000236.2:p.Thr992Ala
CA4448620
NM_000245.4:c.2974A>G