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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CUX2
(V56A)
Single nucleotide variant
(5 prime UTR variant +1 more)
Developmental and epileptic encephalopathy, 67
GUncertain significance
CUX2
(D766H +1 more)
Single nucleotide variant
(missense variant)
Developmental and epileptic encephalopathy, 67
GUncertain significance