Search Results: 1 unique variant retrieved.



Terms with a '*' next to them are explained on the Help Page .

  Undefined cDNA (R68C)
p.Arg68Cys (Legacy AA No. 28)
Variant Type: 
Point
Domain: 
Gla domain
Location: 
Exon 2
Variant Effect: 
Missense
Codon Change: 
No. of Patients Reported: 
0
Phenotype: 
II
Allele Count *: 
-
Allele Number *: 
-
Allele Frequency *: 
-

References and Comments:

Hu et al 2017

Patient Information: Show


Structural Interpretation:

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Factor X Variant Database