Rh > RHCE*03.24 RHCE*cE.24
Allele Information
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Phenotypes
Genetic Changes
nt change aa change Exon/Intron HGVS hg19 hg38 rsNum gnomAD
c.1130A>T p.Ala377Val Exon 8 chr1:25,701,863 chr1:25,375,372
 
Sequence
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