Search Results: 1 unique variant retrieved.
Terms with a '*' next to them are explained on the Help Page .
c.746C>T
p.Ala249Val (Legacy AA No. 221)
Variant Type: 
Point
Domain: 
d5A1
Location: 
Exon 6
Variant Effect: 
Missense
Codon Change: 
746C>T
No. of Patients Reported: 
3
Phenotype: 
Asymptomatic
Association: 
FV Deficiency
Allele Count *: 
NA
Allele Number *: 
NA
Allele Frequency *: 
NA
References and Comments:
Murray et al 1995gum and rectal bleeding; epistaxis