Search Results: 1 unique variant retrieved.
Terms with a '*' next to them are explained on the Help Page .
c.695A>C
p.His232Pro (Legacy AA No. 214)
Variant Type:
Point
Domain:
Apple 3
Codon Change:
A>C
Variant Effect:
Missense
No. of Patients Reported:
1
Phenotype:
U
Allele Count *:
-
Allele Number *:
-
Allele Frequency *:
-