Allele Registry

Canonical Allele Identifier: PA916050226

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV000992056

ClinVar Variation:

804850

HGVS (amino-acid)	Matching Registered Transcripts
NP_277042.1:p.Arg192Gly	CA367401531 NM_033507.3:c.574C>G