Search Results: 1 unique variant retrieved.
Terms with a '*' next to them are explained on the Help Page .
c.646G>A
p.Asp216Asn (Legacy AA No. 198)
Variant Type:
Point
Domain:
Apple 3
Codon Change:
G>A
Variant Effect:
Missense
No. of Patients Reported:
0
Phenotype:
U
Allele Count *:
-
Allele Number *:
-
Allele Frequency *:
-