Allele Registry

Canonical Allele Identifier: PA2827936601

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV000117130

RCV002336252

RCV003318498

RCV003883459

ClinVar Variation:

129143

3024423

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341729.1:p.Gly175Arg	CA231137 NM_001354800.1:c.523G>A CA367401686 NM_001354800.1:c.523G>C