Allele Registry

Canonical Allele Identifier: PA130527

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV000032978

RCV003883126

ClinVar Variation:

39759

HGVS (amino-acid)	Matching Registered Transcripts
NP_000153.1:p.Glu339Lys	CA130526 NM_000162.5:c.1015G>A