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  Search Results: 1 unique variant retrieved.



p.Arg170Cys (Legacy AA No. 110)
Variant Type:
Point
Domain:
EGF2
Sequence Context:
CGC > TGC
Variant Effect:
Missense
Location:
Exon (6)
No of bases:
1
No. of patients reported:
4
Allele Frequency (MAF):

Molecular Graphics and Amino-acid Alignments

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Factor VII Variant Database