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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ATP1A3
(G1005D +2 more)
Single nucleotide variant
(missense variant)
Dystonia 12
+1 more
GUncertain significance
ATP1A3
(R507H +2 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
ATP1A3
(R463H +2 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GConflicting classifications of pathogenicity
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