Allele Registry

Canonical Allele Identifier: PA2827936906

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV000440624

RCV003325955

ClinVar Variation:

381598

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341729.1:p.Val367Met	CA16605802 NM_001354800.1:c.1099G>A