Rh > RHCE*03.21 RHCE*cE.21
Allele Information
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Phenotypes
Genetic Changes
nt change aa change Exon/Intron HGVS hg19 hg38 rsNum gnomAD
c.527C>T p.Ala176Val Exon 4 chr1:25,718,592 chr1:25,392,101
 
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