Canonical Allele Identifier: PA231136
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 129142

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Phe150Tyr
CA231135
NM_000162.5:c.449T>A