Allele Registry

Canonical Allele Identifier: PA2830123501

Gene: GCK HGNC NCBI

ClinVar Variation Id: 995373

HGVS (amino-acid)	Matching Registered Transcripts
NP_277043.1:p.Gly245Glu	CA367400662 NM_033508.3:c.734G>A