Search Results: 1 unique variant retrieved.
Terms with a '*' next to them are explained on the Help Page .
c.224C>T
p.Thr75Ile (Legacy AA No. 57)
Variant Type:
Point
Domain:
Apple 1
Codon Change:
C>T
Variant Effect:
Missense
No. of Patients Reported:
0
Phenotype:
U
Allele Count *:
-
Allele Number *:
-
Allele Frequency *:
-