Allele Registry

Canonical Allele Identifier: PA2827936696

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV003325674

ClinVar Variation:

2578075

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341729.1:p.Gly223Arg	CA367401164 NM_001354800.1:c.667G>C