Allele Registry

Canonical Allele Identifier: PA2827936699

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV000657901

RCV003343982

ClinVar Variation:

546098

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341729.1:p.Ile225Met	CA367401129 NM_001354800.1:c.675C>G