Canonical Allele Identifier: PA2827254234
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 1199923

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311331.1:p.Ser325Arg
CA164894406
NM_001324402.2:c.973A>C
CA368981904
NM_001324402.2:c.975T>A
CA368981911
NM_001324402.2:c.975T>G