Canonical Allele Identifier: PA2827937375
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 995101

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341732.1:p.Gly66Asp
CA367398670
NM_001354803.2:c.197G>A