Search Results: 1 unique variant retrieved.
Terms with a '*' next to them are explained on the Help Page .
c.1631A>G
p.Gln544Arg (Legacy AA No. 516)
Variant Type: 
Point
Domain: 
d5A2
Location: 
Exon 11
Variant Effect: 
Missense
Codon Change: 
1631A>G
No. of Patients Reported: 
1
Phenotype: 
NA
Association: 
thrombosis
Allele Count *: 
NA
Allele Number *: 
NA
Allele Frequency *: 
NA
References and Comments:
Abdi et al 2017NA