Allele Registry

Canonical Allele Identifier: PA2830123581

Gene: GCK HGNC NCBI

ClinVar Variation Id: 447420

HGVS (amino-acid)	Matching Registered Transcripts
NP_277043.1:p.Glu267Lys	CA367400529 NM_033508.3:c.799G>A