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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TRRAP
(P822L)
Single nucleotide variant
(missense variant)
See cases
+1 more
GUncertain significance
TRRAP
(V1363I)
Single nucleotide variant
(missense variant)
See cases
+1 more
GUncertain significance
TRRAP
Single nucleotide variant
(intron variant)
not provided
+1 more
GConflicting classifications of pathogenicity
TRRAP
(V1883I +2 more)
Single nucleotide variant
(missense variant)
See cases
GLikely pathogenic
TRRAP
(A3421S +2 more)
Single nucleotide variant
(missense variant)
See cases
GUncertain significance
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