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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
RHOA
(R148K +3 more)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
RHOA
(R48H +1 more)
Single nucleotide variant
(missense variant +2 more)
not provided
GUncertain significance
RHOA
(A61T)
Single nucleotide variant
(missense variant +2 more)
not provided
GUncertain significance
RHOA
(E47K)
Single nucleotide variant
(missense variant +2 more)
neuro-ectodermal phenotype
+3 more
GPathogenic
ABHD5, ACAA1
+177 more
Copy number gain
See cases
GLikely pathogenic
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