Kx > XK*N.17
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Phenotypes
Genetic Changes
nt change aa change Exon/Intron HGVS hg19 hg38 rsNum gnomAD
c.397C>T Exon 2 chrX:37,553,710 chrX:37,694,457
 
 
 
 
 
 
 
 
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