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  Search Results: 1 unique variant retrieved.



  c.3196C>T
p.(His1066Tyr) (Legacy AA No.1047)
Variant Type:
Point
Domain:
B
Sequence Context:
CAT > TAT
Variant Effect:
Missense
Location:
Exon 14
No of bases:
1
No. of cases reported:
1
Allele Frequency (MAF):

Molecular Graphics and Amino-acid Alignments

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