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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CLTC
(I40V)
Single nucleotide variant
(missense variant)
Intellectual disability, autosomal dominant 56
GUncertain significance
CLTC
(R399H +1 more)
Single nucleotide variant
(missense variant)
Intellectual disability, autosomal dominant 56
GUncertain significance
CLTC
(P485L +1 more)
Single nucleotide variant
(missense variant)
Intellectual disability, autosomal dominant 56
GUncertain significance
CLTC
(M1592V +1 more)
Single nucleotide variant
(missense variant)
Intellectual disability, autosomal dominant 56
+2 more
GConflicting classifications of pathogenicity
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