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  Search Results: 1 unique variant retrieved.



  c.1163T>C
p.(Ile388Thr) (Legacy AA No.369)
Variant Type:
Point
Domain:
a1
Sequence Context:
ATC > ACC
Variant Effect:
Missense
Location:
Exon 8
No of bases:
1
No. of cases reported:
8
Allele Frequency (MAF):

Molecular Graphics and Amino-acid Alignments

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