Allele Registry

Canonical Allele Identifier: PA2827936885

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV000032978

RCV003883126

ClinVar Variation:

39759

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341729.1:p.Glu339Lys	CA130526 NM_001354800.1:c.1015G>A