Search Results: 1 unique variant retrieved.
Terms with a '*' next to them are explained on the Help Page .
c.865G>C
p.Gly289Arg (Legacy AA No. 249)
Variant Type:
Point
Domain:
Serine protease
Location:
Exon 7
Variant Effect:
Missense
Codon Change:
G>C
No. of Patients Reported:
3
Phenotype:
U
Allele Count *:
-
Allele Number *:
-
Allele Frequency *:
-