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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CLCN7
(A764T +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
CLCN7
(R688G +1 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
CLCN7
(I506L +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
CLCN7
(N138S +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
CLCN7
(R102C +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
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