Allele Registry

Canonical Allele Identifier: PA2830124061

Gene: GCK HGNC NCBI

ClinVar Variation Id: 521398

HGVS (amino-acid)	Matching Registered Transcripts
NP_277043.1:p.Glu441Lys	CA4239377 NM_033508.3:c.1321G>A