U.S. flag

An official website of the United States government

Format
Sort by
Choose Destination

Search results

Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KCTD7
(G58R)
Single nucleotide variant
(missense variant)
Progressive myoclonic epilepsy type 3
GUncertain significance
KCTD7
(A178V)
Single nucleotide variant
(missense variant)
Progressive myoclonic epilepsy type 3
GConflicting classifications of pathogenicity