Allele Registry

Canonical Allele Identifier: PA2830122278

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV001288975

RCV003330326

ClinVar Variation:

995102

HGVS (amino-acid)	Matching Registered Transcripts
NP_277042.1:p.Arg398His	CA367398533 NM_033507.3:c.1193G>A