Allele Registry

Canonical Allele Identifier: PA2579980349

Gene: GCK HGNC NCBI

ClinVar Variation Id: 447420

HGVS (amino-acid)	Matching Registered Transcripts
NP_000153.1:p.Glu268Lys	CA367400529 NM_000162.5:c.802G>A