Allele Registry

Canonical Allele Identifier: PA2830123748

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV000032978

RCV003883126

ClinVar Variation:

39759

HGVS (amino-acid)	Matching Registered Transcripts
NP_277043.1:p.Glu338Lys	CA130526 NM_033508.3:c.1012G>A