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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
RANBP2
(L259V)
Single nucleotide variant
(missense variant)
Familial acute necrotizing encephalopathy
GUncertain significance
RANBP2
(I656V)
Single nucleotide variant
(missense variant)
Familial acute necrotizing encephalopathy
GConflicting classifications of pathogenicity
RANBP2
(K1121N)
Single nucleotide variant
(missense variant)
Familial acute necrotizing encephalopathy
GConflicting classifications of pathogenicity
RANBP2
(D2375E)
Single nucleotide variant
(missense variant)
Familial acute necrotizing encephalopathy
GUncertain significance
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