Search Results: 1 unique variant retrieved.
Terms with a '*' next to them are explained on the Help Page .
c.1219A>C
p.Thr407Pro (Legacy AA No. 389)
Variant Type: 
Point
Domain: 
Serine Protease
Codon Change: 
A>C
Variant Effect: 
Missense
No. of Patients Reported: 
1
Phenotype: 
U
Allele Count *: 
-
Allele Number *: 
-
Allele Frequency *: 
-