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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KCNH5
Single nucleotide variant
(synonymous variant +1 more)
Early infantile epileptic encephalopathy with suppression bursts
+1 more
GBenign
KCNH5
Single nucleotide variant
(synonymous variant)
Early infantile epileptic encephalopathy with suppression bursts
+1 more
GBenign/Likely benign
KCNH5
Single nucleotide variant
(intron variant)
Early infantile epileptic encephalopathy with suppression bursts
+2 more
GBenign
KCNH5
(I366M)
Single nucleotide variant
(missense variant)
KCNH5-related condition
+1 more
GBenign/Likely benign
KCNH5
Duplication
(intron variant)
Early infantile epileptic encephalopathy with suppression bursts
+1 more
GBenign/Likely benign
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