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  Search Results: 1 unique variant retrieved.



  c.6113A>G
p.(Asn2038Ser) (Legacy AA No.2019)
Variant Type:
Point
Domain:
A3
Sequence Context:
AAT > AGT
Variant Effect:
Missense
Location:
Exon 19
No of bases:
1
No. of cases reported:
19
Allele Frequency (MAF):

Molecular Graphics and Amino-acid Alignments

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