Allele Registry

Canonical Allele Identifier: PA658819830

Gene: GCK HGNC NCBI

ClinVar Variation Id: 521398

HGVS (amino-acid)	Matching Registered Transcripts
NP_277042.1:p.Glu443Lys	CA4239377 NM_033507.3:c.1327G>A