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VWF S1731L multimer [extracellular region]
Stable Identifier
R-HSA-9823688
Type
Complex
Species
Homo sapiens
Compartment
extracellular region
Synonyms
von Willibrand factor multimer
Locations in the PathwayBrowser
Expand all
Disease (Homo sapiens)
Diseases of hemostasis (Homo sapiens)
Defects of platelet adhesion to exposed collagen (Homo sapiens)
Defective VWF binding to collagen type I (Homo sapiens)
VWF variant does not bind to collagen type I (Homo sapiens)
VWF A3 domain variant multimer [extracellular region] (Homo sapiens)
VWF S1731L multimer [extracellular region] (Homo sapiens)
Participants
components
x 50
VWF S1731L (764-2813) [extracellular region]
(Homo sapiens)
Participates
as a candidate of
VWF A3 domain variant multimer [extracellular region] (Homo sapiens)
Disease
Name
Identifier
Synonyms
blood platelet disease
DOID:2218
platelet disorder, Thrombocytopathy
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