Allele Registry

Canonical Allele Identifier: PA2827937297

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV001288975

RCV003330326

ClinVar Variation:

995102

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341731.1:p.Arg17His	CA367398533 NM_001354802.1:c.50G>A