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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
RHOBTB2
(V19A +2 more)
Single nucleotide variant
(missense variant)
Developmental and epileptic encephalopathy, 64
GUncertain significance
RHOBTB2
(W217C +2 more)
Single nucleotide variant
(missense variant)
Developmental and epileptic encephalopathy, 64
GUncertain significance
RHOBTB2
(R511W +2 more)
Single nucleotide variant
(missense variant)
Rett syndrome
+3 more
GPathogenic/Likely pathogenic
RHOBTB2
(D568Y +2 more)
Single nucleotide variant
(missense variant)
Developmental and epileptic encephalopathy, 64
GUncertain significance
RHOBTB2
(W708S +2 more)
Single nucleotide variant
(missense variant)
Developmental and epileptic encephalopathy, 64
GUncertain significance
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