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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TPP2
Single nucleotide variant
(intron variant)
Evans syndrome, immunodeficiency, and premature immunosenescence associated with tripeptidyl-peptidase II deficiency
GUncertain significance
TPP2
(K864R)
Single nucleotide variant
(missense variant +1 more)
Evans syndrome, immunodeficiency, and premature immunosenescence associated with tripeptidyl-peptidase II deficiency
GUncertain significance