Allele Registry

Canonical Allele Identifier: PA2830122736

Gene: GCK HGNC NCBI

ClinVar Variation Id: 1299600

HGVS (amino-acid)	Matching Registered Transcripts
NP_277043.1:p.Glu47Lys	CA4239714 NM_033508.3:c.139G>A