RF Logo The European Association for Haemophilia and Allied Disorders Factor VII Variant Database EAHAD Coagulation Variant Databases

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  Search Results: 1 unique variant retrieved.



  c.6140C>G
p.(Ala2047Gly) (Legacy AA No.2028)
Variant Type:
Point
Domain:
C1
Sequence Context:
GGT > GCT
Variant Effect:
Missense
Location:
Exon 20
No of bases:
No. of cases reported:
1
Allele Frequency (MAF):

Molecular Graphics and Amino-acid Alignments

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Individual Case Information : Show