The association between KCNA2 (Potassium Voltage-Gated Channel Subfamily A Member 2) and Developmental And Epileptic Encephalopathy 32 is well established and manually curated, with its 4 contributing sources — 3 of them expert-curated — recording a known molecular basis, pathogenic variants, and causative variation.
Sources4
Clinical variants416
Symptoms18
Compounds0
Trials0
Publications17
01
At a glance
Association overview
A cited synthesis of the gene–disorder association, with a clinical-actionability summary where the evidence supports one.