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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ATP1A3
(G947R +2 more)
Single nucleotide variant
(missense variant)
Dystonia 12
+4 more
GPathogenic
ATP1A3
(T613M +2 more)
Single nucleotide variant
(missense variant)
Alternating hemiplegia of childhood 2
+2 more
GPathogenic