Search Results: 1 unique variant retrieved.
Terms with a '*' next to them are explained on the Help Page .
c.198G>C
p.Glu66Asp (Legacy AA No. 26)
Variant Type:
Point
Domain:
Gla domain
Location:
Exon 2
Variant Effect:
Missense
Codon Change:
G>C
No. of Patients Reported:
0
Phenotype:
U
Allele Count *:
-
Allele Number *:
-
Allele Frequency *:
-