Allele Registry

Canonical Allele Identifier: PA2830122804

Gene: GCK HGNC NCBI

ClinVar Variation Id: 1679552

HGVS (amino-acid)	Matching Registered Transcripts
NP_277043.1:p.Glu69Lys	CA367403203 NM_033508.3:c.205G>A