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  Search Results: 1 unique variant retrieved.



  c.6944C>T
p.(Ser2315Phe) (Legacy AA No.2296)
Variant Type:
Point
Domain:
C2
Sequence Context:
TCT > TTT
Variant Effect:
Missense
Location:
Exon 26
No of bases:
No. of cases reported:
1
Allele Frequency (MAF):

Molecular Graphics and Amino-acid Alignments

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