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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ATP1A3
(G867V +2 more)
Single nucleotide variant
(missense variant)
Developmental and epileptic encephalopathy 99
GUncertain significance
ATP1A3
(E815K +2 more)
Single nucleotide variant
(missense variant)
Alternating hemiplegia of childhood 2
+13 more
GPathogenic