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Search Results: 1 unique variant retrieved.
p.Ala51Asp (Legacy AA No. -9)
Variant Type:
Point
Domain:
Propeptide
Sequence Context:
GAC > GCC
Variant Effect:
Missense
Location:
Exon (3)
No of bases:
1
No. of patients reported:
1
Allele Frequency (MAF):
Molecular Graphics and Amino-acid Alignments
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