Allele Registry

Canonical Allele Identifier: PA2579982050

Gene: GCK HGNC NCBI

ClinVar Variation Id: 872751

HGVS (amino-acid)	Matching Registered Transcripts
NP_000153.1:p.Arg377Leu	CA367398811 NM_000162.5:c.1130G>T