Allele Registry

Canonical Allele Identifier: PA645460342

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV000445412

ClinVar Variation:

393450

HGVS (amino-acid)	Matching Registered Transcripts
NP_277042.1:p.Glu340Gly	CA16609267 NM_033507.3:c.1019A>G