Allele Registry

Canonical Allele Identifier: PA2830123785

Gene: GCK HGNC NCBI

ClinVar Variation Id: 129140

HGVS (amino-acid)	Matching Registered Transcripts
NP_277043.1:p.Cys370Phe	CA152950 NM_033508.3:c.1109G>T