Search Results: 1 unique variant retrieved.
Terms with a '*' next to them are explained on the Help Page .
c.723C>G
p.Phe241Leu (Legacy AA No. 223)
Variant Type:
Point
Domain:
Apple 3
Codon Change:
C>G
Variant Effect:
Missense
No. of Patients Reported:
0
Phenotype:
U
Allele Count *:
19
Allele Number *:
282784
Allele Frequency *:
0.000067