Search Results: 1 unique variant retrieved.
Terms with a '*' next to them are explained on the Help Page .
c.413A>T
p.Gln138Leu (Legacy AA No. 98)
Variant Type:
Point
Domain:
EGF-2
Location:
Exon 5
Variant Effect:
Missense
Codon Change:
A>T
No. of Patients Reported:
0
Phenotype:
U
Allele Count *:
-
Allele Number *:
-
Allele Frequency *:
-