Allele Registry

Canonical Allele Identifier: PA2830123568

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV000029921

RCV000117135

RCV000517906

RCV000826166

RCV002467500

ClinVar Variation:

36258

HGVS (amino-acid)	Matching Registered Transcripts
NP_277043.1:p.Ser262Pro	CA152961 NM_033508.3:c.784T>C