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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KCND3
(T377M)
Single nucleotide variant
(missense variant)
Spinocerebellar ataxia type 19/22
+1 more
GPathogenic
KCND3
(P375S)
Single nucleotide variant
(missense variant)
Spinocerebellar ataxia type 19/22
GPathogenic
KCND3
(V338E)
Single nucleotide variant
(missense variant)
Spinocerebellar ataxia type 19/22
GPathogenic
KCND3
(C317Y)
Single nucleotide variant
(missense variant)
Spinocerebellar ataxia type 19/22
GPathogenic
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