F7 wt Allele

**Semantic type:** Gene or Genome

**Definition:** Human F7 wild-type allele is located within 13q34 and is approximately 14 kb in length. This allele, which encodes coagulation factor VII protein, plays a role in homeostasis and blood coagulation. Defects in the gene associated with variant alleles are causative agents for coagulopathy.

**Synonyms:** - Coagulation Factor VII (Serum Prothrombin Conversion Accelerator) wt Allele - FA7 - SPCA