Allele Registry

Canonical Allele Identifier: PA891855359

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV000711758

RCV002285406

RCV003318504

RCV003420270

ClinVar Variation:

585909

HGVS (amino-acid)	Matching Registered Transcripts
NP_277042.1:p.Arg393Cys	CA367398622 NM_033507.3:c.1177C>T