Search Results: 1 unique variant retrieved.
Terms with a '*' next to them are explained on the Help Page .
c.271T>A
p.Tyr91Asn (Legacy AA No. 63)
Variant Type:
Point
Domain:
d5A1
Location:
Exon 3
Variant Effect:
Missense
Codon Change:
271T>A
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 2009bleeding after invasive procedure, epistaxis; haematoma