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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SCN8A
(I142V)
Single nucleotide variant
(missense variant)
not provided
+2 more
GConflicting classifications of pathogenicity
SCN8A
(A1491V +1 more)
Single nucleotide variant
(missense variant)
not provided
GPathogenic
SCN8A
(T1787N +1 more)
Single nucleotide variant
(missense variant)
Early infantile epileptic encephalopathy with suppression bursts
+1 more
GConflicting classifications of pathogenicity
SCN8A
(R1872W +1 more)
Single nucleotide variant
(missense variant)
not provided
+4 more
GPathogenic
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