Submit Variant


Our Center would like to learn about interesting ion channel variants associated with epilepsy or related neurodevelopmental disorders. You may nominate a variant for consideration by our research teams. We are particularly interested in novel variants associated with unique clinical features (phenotype) including drug responses. Variants with available clinical information will be given highest priority. Please do not include any personal identifying information such as names, birthdates, addresses of the individual with the variant.

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e.g. KCNQ2

e.g. c.638G>A

e.g. p.Arg213Gln

(if known) e.g. NM_172107.3