Allele Registry

Canonical Allele Identifier: PA2579975561

Gene: GCK HGNC NCBI

ClinVar Variation Id: 447413

HGVS (amino-acid)	Matching Registered Transcripts
NP_000153.1:p.Thr228Ala	CA367400790 NM_000162.5:c.682A>G