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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ALG13
(V77A)
Single nucleotide variant
(missense variant +3 more)
Developmental and epileptic encephalopathy, 36
GUncertain significance
ALG13
(N107S +3 more)
Single nucleotide variant
(missense variant +2 more)
not provided
+5 more
GPathogenic
ALG13
(E300K +2 more)
Single nucleotide variant
(missense variant +1 more)
Developmental and epileptic encephalopathy, 36
GConflicting classifications of pathogenicity
ALG13
Microsatellite
(inframe_insertion +1 more)
Developmental and epileptic encephalopathy, 36
+1 more
GBenign/Likely benign
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