Allele Registry

Canonical Allele Identifier: PA2825042500

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV001288975

RCV003330326

ClinVar Variation:

995102

HGVS (amino-acid)	Matching Registered Transcripts
NP_000153.1:p.Arg397His	CA367398533 NM_000162.5:c.1190G>A