Canonical Allele Identifier: PA2499249418
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 1199923

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311330.1:p.Ser755Arg
CA164894406
NM_001324401.3:c.2263A>C
CA368981904
NM_001324401.3:c.2265T>A
CA368981911
NM_001324401.3:c.2265T>G