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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
HCN1
(T650P)
Single nucleotide variant
(missense variant)
Developmental and epileptic encephalopathy, 24
GUncertain significance
HCN1
(R549H)
Single nucleotide variant
(missense variant)
Generalized epilepsy with febrile seizures plus, type 10
+1 more
GUncertain significance
HCN1
(M94I)
Single nucleotide variant
(missense variant)
Early infantile epileptic encephalopathy with suppression bursts
+1 more
GConflicting classifications of pathogenicity
HCN1
(A25E)
Single nucleotide variant
(missense variant)
Early infantile epileptic encephalopathy with suppression bursts
+1 more
GConflicting classifications of pathogenicity
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