Canonical Allele Identifier: PA916027580
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 446117

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311331.1:p.Tyr804Cys
CA368991650
NM_001324402.2:c.2411A>G