Canonical Allele Identifier: PA1139749042
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 995373

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Gly247Glu
CA367400662
NM_033507.3:c.740G>A