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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KCNC1
(H480N)
Single nucleotide variant
(missense variant)
Progressive myoclonic epilepsy type 7
GUncertain significance
KCNC1
(L532Q)
Single nucleotide variant
(missense variant)
Seizure
GUncertain significance