Search Results: 1 unique variant retrieved.
Terms with a '*' next to them are explained on the Help Page .
c.2051G>A
p.Cys684Tyr (Legacy AA No. 656)
Variant Type:
Point
Domain:
d5a2
Location:
Exon 13
Variant Effect:
Missense
Codon Change:
2051G>A
No. of Patients Reported:
1
Phenotype:
NA
Association:
FV Deficiency
Allele Count *:
NA
Allele Number *:
NA
Allele Frequency *:
NA
References and Comments:
Cao et al 2008NA