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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SCN3A
(Q557L)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
SCN3A
(A433V)
Single nucleotide variant
(missense variant)
Developmental and epileptic encephalopathy, 62
GUncertain significance