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
CSTB, LOC130066788
(Q10P)
Single nucleotide variant
(missense variant)
Progressive myoclonic epilepsy
+1 more
GUncertain significance
CSTB, LOC130066788
Single nucleotide variant
(synonymous variant)
Inborn genetic diseases
+3 more
GBenign/Likely benign