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Items: 7

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TTPA
(S272R)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
TTPA
(D185E)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
TTPA
Single nucleotide variant
(intron variant)
not provided
GConflicting classifications of pathogenicity
TTPA
Deletion
(intron variant)
not specified
+2 more
GBenign
TTPA
(D60N)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
TTPA
Single nucleotide variant
(synonymous variant)
not provided
+2 more
GBenign/Likely benign
TTPA
Single nucleotide variant
(synonymous variant)
not specified
+2 more
GBenign
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