Allele Registry

Canonical Allele Identifier: PA2830123885

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV000029844

RCV003883122

ClinVar Variation:

36181

HGVS (amino-acid)	Matching Registered Transcripts
NP_277043.1:p.Ala386Glu	CA213725 NM_033508.3:c.1157C>A