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  Search Results: 1 unique variant retrieved.



  c.6437T>C
p.(Phe2146Ser) (Legacy AA No.2127)
Variant Type:
Point
Domain:
C1
Sequence Context:
TTT > TCT
Variant Effect:
Missense
Location:
Exon 23
No of bases:
1
No. of cases reported:
34
Allele Frequency (MAF):

Molecular Graphics and Amino-acid Alignments

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