Canonical Allele Identifier: PA645461096
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36199

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Ala450Thr
CA213758
NM_033507.3:c.1348G>A