Allele Registry

Canonical Allele Identifier: PA2827937094

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV000440624

RCV003325955

ClinVar Variation:

381598

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341730.1:p.Val30Met	CA16605802 NM_001354801.1:c.88G>A