Allele Registry

Canonical Allele Identifier: PA2580490812

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV003060103

RCV003329455

ClinVar Variation:

2136518

HGVS (amino-acid)	Matching Registered Transcripts
NP_277042.1:p.Gly228Ser	CA367401117 NM_033507.3:c.682G>A