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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
F13A1
(G593S)
Single nucleotide variant
(missense variant)
not specified
+1 more
GConflicting classifications of pathogenicity
F13A1
(T577M)
Single nucleotide variant
(missense variant)
Factor XIII, A subunit, deficiency of
+1 more
GConflicting classifications of pathogenicity
F13A1
(A395V)
Single nucleotide variant
(missense variant)
not specified
+2 more
GConflicting classifications of pathogenicity
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