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  Search Results: 1 unique variant retrieved.



  c.505G>A
p.(Asp169Asn) (Legacy AA No.150)
Variant Type:
Point
Domain:
A1
Sequence Context:
GAC > AAC
Variant Effect:
Missense
Location:
Exon 4
No of bases:
No. of cases reported:
1
Allele Frequency (MAF):

Molecular Graphics and Amino-acid Alignments

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