Canonical Allele Identifier: PA257005
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 13885

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120972.1:p.Tyr1248Cys
CA257003
NM_001127500.3:c.3743A>G