Allele Registry

Canonical Allele Identifier: PA2827937359

Gene: GCK HGNC NCBI

ClinVar Variation Id: 219179

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341732.1:p.Asp22Tyr	CA279947 NM_001354803.2:c.64G>T