Canonical Allele Identifier: PA2826672170
Gene: RHD HGNC NCBI
ClinVar Allele:
32751
ClinVar RCV:
RCV000019286
ClinVar Variation:
17712
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269801.1:p.Leu110Pro
CA127334
NM_001282872.1:c.329T>C