Allele Registry

Canonical Allele Identifier: PA2830123455

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV003060103

RCV003329455

ClinVar Variation:

2136518

HGVS (amino-acid)	Matching Registered Transcripts
NP_277043.1:p.Gly226Ser	CA367401117 NM_033508.3:c.676G>A