Search Results: 1 unique variant retrieved.
Terms with a '*' next to them are explained on the Help Page .
c.259C>A
p.Pro87Thr (Legacy AA No. 69)
Variant Type:
Point
Domain:
Apple 1
Codon Change:
C>A
Variant Effect:
Missense
No. of Patients Reported:
1
Phenotype:
I
Allele Count *:
-
Allele Number *:
-
Allele Frequency *:
-