Allele Registry

Canonical Allele Identifier: PA2830123434

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV003060105

ClinVar Variation:

2136520

HGVS (amino-acid)	Matching Registered Transcripts
NP_277043.1:p.Gly222Val	CA367401157 NM_033508.3:c.665G>T