Canonical Allele Identifier: PA916027468
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 216499

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311331.1:p.His54Arg
CA339400
NM_001324402.2:c.161A>G