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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ATP1A2
(A283V)
Single nucleotide variant
(missense variant)
Familial hemiplegic migraine
+1 more
GConflicting classifications of pathogenicity
ATP1A2
(E1000K)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance