Allele Registry

Canonical Allele Identifier: PA2830123295

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV000992056

ClinVar Variation:

804850

HGVS (amino-acid)	Matching Registered Transcripts
NP_277043.1:p.Arg190Gly	CA367401531 NM_033508.3:c.568C>G