Allele Registry

Canonical Allele Identifier: PA658669149

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV000516548

RCV004527381

ClinVar Variation:

447386

HGVS (amino-acid)	Matching Registered Transcripts
NP_277042.1:p.Gly411Asp	CA367398309 NM_033507.3:c.1232G>A