Rh > RHCE*01N.08 RHCE*ceN.08
Allele Information
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Phenotypes
Genetic Changes
nt change aa change Exon/Intron HGVS hg19 hg38 rsNum gnomAD
c.801+1G>A silent Intron 5 chr1:25,717,239 chr1:25,390,748
 
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