Allele Registry

Canonical Allele Identifier: PA2830122316

Gene: GCK HGNC NCBI

ClinVar Variation Id: 985725

HGVS (amino-acid)	Matching Registered Transcripts
NP_277042.1:p.Gly408Ser	CA367398357 NM_033507.3:c.1222G>A