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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KCNH5
(L690R)
Single nucleotide variant
(missense variant +1 more)
Early infantile epileptic encephalopathy with suppression bursts
+1 more
GUncertain significance
KCNH5
(V36M)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance