Allele Registry

Canonical Allele Identifier: PA645460345

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV000032978

RCV003883126

ClinVar Variation:

39759

HGVS (amino-acid)	Matching Registered Transcripts
NP_277042.1:p.Glu340Lys	CA130526 NM_033507.3:c.1018G>A