Canonical Allele Identifier: PA2826672079
Gene: RHD HGNC NCBI

Linked Data

ClinVar Variation Id: 242592
ClinVar RCV Id: RCV000515751 RCV000515752
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269796.1:p.Gly189Ser
CA354106
NM_001282867.1:c.565G>A