Allele Registry

Canonical Allele Identifier: PA916039359

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV000029844

RCV003883122

ClinVar Variation:

36181

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341731.1:p.Ala7Glu	CA213725 NM_001354802.1:c.20C>A