Canonical Allele Identifier: PA916027544
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 13881

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311331.1:p.Met701Thr
CA256991
NM_001324402.2:c.2102T>C