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Links from MedGen

Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
F13A1
(W188L)
Single nucleotide variant
(missense variant)
Hereditary factor XIII deficiency disease
GPathogenic
F13B
(E388V)
Single nucleotide variant
(missense variant)
Hereditary factor XIII deficiency disease
+2 more
GUncertain significance