Canonical Allele Identifier: PA916027575
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 13884

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311331.1:p.Asp798Asn
CA257000
NM_001324402.2:c.2392G>A