Allele Registry

Canonical Allele Identifier: PA2830123901

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV000711758

RCV002285406

RCV003318504

RCV003420270

ClinVar Variation:

585909

HGVS (amino-acid)	Matching Registered Transcripts
NP_277043.1:p.Arg391Cys	CA367398622 NM_033508.3:c.1171C>T