Allele Registry

Canonical Allele Identifier: PA096536

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV000440624

RCV003325955

ClinVar Variation:

381598

HGVS (amino-acid)	Matching Registered Transcripts
NP_000153.1:p.Val367Met	CA16605802 NM_000162.5:c.1099G>A