Allele Registry

Canonical Allele Identifier: PA2827936971

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV000711758

RCV002285406

RCV003318504

RCV003420270

ClinVar Variation:

585909

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341729.1:p.Arg392Cys	CA367398622 NM_001354800.1:c.1174C>T