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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KCNA2
(R419W)
Single nucleotide variant
(missense variant +1 more)
Developmental and epileptic encephalopathy, 32
+1 more
GUncertain significance
KCNA2
(R297W)
Single nucleotide variant
(missense variant)
Developmental and epileptic encephalopathy, 32
+1 more
GPathogenic
KCNA2
(Q214K)
Single nucleotide variant
(missense variant)
Developmental and epileptic encephalopathy, 32
GUncertain significance
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