Allele Registry

Canonical Allele Identifier: PA2825075839

Gene: GCK HGNC NCBI

ClinVar Variation Id: 1299600

HGVS (amino-acid)	Matching Registered Transcripts
NP_000153.1:p.Glu48Lys	CA4239714 NM_000162.5:c.142G>A