Allele Registry

Canonical Allele Identifier: PA2830123482

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV000117134

ClinVar Variation:

129146

HGVS (amino-acid)	Matching Registered Transcripts
NP_277043.1:p.Glu235Lys	CA152959 NM_033508.3:c.703G>A