Allele Registry

Canonical Allele Identifier: PA2827937248

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV000017520

RCV002513079

ClinVar Variation:

16140

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341730.1:p.Val118Met	CA257432 NM_001354801.1:c.352G>A