Search Results: 1 unique variant retrieved.
c.1982T>A
p.(Ile661Asn ) (Legacy AA No.642)
Variant Type:
Point
Domain:
A2
Sequence Context:
ATT > AAT
Variant Effect:
Missense
Location:
Exon 13
No of bases:
No. of cases reported:
1
Allele Frequency (MAF):
Molecular Graphics and Amino-acid Alignments
Individual Case Information :
Show