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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CAD
(Q444R)
Single nucleotide variant
(missense variant)
Developmental and epileptic encephalopathy, 50
GUncertain significance
CAD
(I1524T +1 more)
Single nucleotide variant
(missense variant)
Developmental and epileptic encephalopathy, 50
+1 more
GUncertain significance
CAD
(P1710R +1 more)
Single nucleotide variant
(missense variant)
Developmental and epileptic encephalopathy, 50
GUncertain significance
CAD
(R1810Q +1 more)
Single nucleotide variant
(missense variant)
Developmental and epileptic encephalopathy, 50
+2 more
GPathogenic/Likely pathogenic
CAD, LOC126806172
(R2059H +1 more)
Single nucleotide variant
(missense variant)
Developmental and epileptic encephalopathy, 50
+1 more
GUncertain significance
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