Search Results: 1 unique variant retrieved.
Terms with a '*' next to them are explained on the Help Page .
c.829G>A
p.Gly277Ser (Legacy AA No. 259)
Variant Type:
Point
Domain:
Apple 3
Codon Change:
G>A
Variant Effect:
Missense
No. of Patients Reported:
1
Phenotype:
I
Allele Count *:
-
Allele Number *:
-
Allele Frequency *:
-