Rh > RHCE*02.35 RHCE*Ce.35
Allele Information
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Phenotypes
Genetic Changes
nt change aa change Exon/Intron HGVS hg19 hg38 rsNum gnomAD
c.491A>G p.Asp164Gly Exon 4 chr1:25,718,628 chr1:25,392,137
 
Sequence
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