Allele Registry

Canonical Allele Identifier: PA2827937372

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV000029844

RCV003883122

ClinVar Variation:

36181

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341732.1:p.Ala65Glu	CA213725 NM_001354803.2:c.194C>A