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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
USP19
(V542L +15 more)
Single nucleotide variant
(missense variant)
Epileptic encephalopathy
GPathogenic
USP19
(E512D +15 more)
Single nucleotide variant
(missense variant)
Epileptic encephalopathy
GPathogenic