Canonical Allele Identifier: PA2826672100
Gene: RHD HGNC NCBI

Linked Data

ClinVar Variation Id: 17713
ClinVar RCV Id: RCV000019287
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269797.1:p.Val270Gly
CA127336
NM_001282868.1:c.809T>G