Rh > RHCE*01.42 RHCE*ce42
Allele Information
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Phenotypes
Genetic Changes
nt change aa change Exon/Intron HGVS hg19 hg38 rsNum gnomAD
c.508A>G p.Arg170Gly Exon 4 chr1:25,718,611 chr1:25,392,120
 
Sequence
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