Allele Registry

Canonical Allele Identifier: PA2827936755

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV000029915

RCV002472937

ClinVar Variation:

36252

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341729.1:p.Val253Ala	CA213842 NM_001354800.1:c.758T>C