Allele Registry

Canonical Allele Identifier: PA2830123526

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV000029915

RCV002472937

ClinVar Variation:

36252

HGVS (amino-acid)	Matching Registered Transcripts
NP_277043.1:p.Val252Ala	CA213842 NM_033508.3:c.755T>C