Search Results: 1 unique variant retrieved.
Terms with a '*' next to them are explained on the Help Page .
c.1064C>T
p.Ala355Val (Legacy AA No. 327)
Variant Type: 
Point
Domain: 
d5A2
Location: 
Exon 7
Variant Effect: 
Missense
Codon Change: 
1064C>T
No. of Patients Reported: 
1
Phenotype: 
Asymptomatic
Association: 
FV Deficiency
Allele Count *: 
NA
Allele Number *: 
NA
Allele Frequency *: 
NA
References and Comments:
Delev et al 2009NA