Search Results: 1 unique variant retrieved.
Terms with a '*' next to them are explained on the Help Page .
c.653T>C
p.Phe218Ser (Legacy AA No. 190)
Variant Type: 
Point
Domain: 
d5A1
Location: 
Exon 5
Variant Effect: 
Missense
Codon Change: 
653T>C
No. of Patients Reported: 
5
Phenotype: 
Mild
Association: 
FV Deficiency
Allele Count *: 
NA
Allele Number *: 
NA
Allele Frequency *: 
NA
References and Comments:
Kanaji et al 2009age 80