Allele Registry

Canonical Allele Identifier: PA2827936698

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV001942615

ClinVar Variation:

1365290

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341729.1:p.Ile225Thr	CA367401133 NM_001354800.1:c.674T>C