Allele Registry

Canonical Allele Identifier: PA2830123929

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV001288975

RCV003330326

ClinVar Variation:

995102

HGVS (amino-acid)	Matching Registered Transcripts
NP_277043.1:p.Arg396His	CA367398533 NM_033508.3:c.1187G>A