Allele Registry

Canonical Allele Identifier: PA152962

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV000029921

RCV000117135

RCV000517906

RCV000826166

RCV002467500

ClinVar Variation:

36258

HGVS (amino-acid)	Matching Registered Transcripts
NP_000153.1:p.Ser263Pro	CA152961 NM_000162.5:c.787T>C