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  Search Results: 1 unique variant retrieved.



  c.2026A>T
p.(Thr676Ser) (Legacy AA No.657)
Variant Type:
Point
Domain:
A2
Sequence Context:
ACC > TCC
Variant Effect:
Missense
Location:
Exon 13
No of bases:
1
No. of cases reported:
2
Allele Frequency (MAF):

Molecular Graphics and Amino-acid Alignments

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