Canonical Allele Identifier: PA916027251
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 141889

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311330.1:p.Asp208Gly
CA166710
NM_001324401.3:c.623A>G