F8 thrombin cleavage site variant [extracellular region]

Stable Identifier
R-HSA-9667118
Type
Set [DefinedSet]
Species
Homo sapiens
Compartment
extracellular region
Synonyms
FVIII thrombin cleavage site variant
Locations in the PathwayBrowser
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Participants
members
Participates
as a component of
Disease
Name Identifier Synonyms
factor VIII deficiency DOID:12134 Congenital factor VIII disorder, Subhemophilia, Hemophilia A
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