Canonical Allele Identifier: PA915966745
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 645086

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120972.1:p.Thr805Ala
CA368982573
NM_001127500.3:c.2413A>G