F8 thrombin cleavage site variant [extracellular region]

Stable Identifier
R-HSA-9667118
Type
Set [DefinedSet]
Species
Homo sapiens
Compartment
Synonyms
FVIII thrombin cleavage site variant
Locations in the PathwayBrowser
Participants
Participant Of
Disease
Name Identifier Synonyms
factor VIII deficiency 12134 Congenital factor VIII disorder, Subhemophilia, Hemophilia A
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