Canonical Allele Identifier: PA916027209
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 246642

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311330.1:p.Val121Ala
CA10584669
NM_001324401.3:c.362T>C