Canonical Allele Identifier: PA2826672188
Gene: RHD HGNC NCBI

Linked Data

ClinVar Variation Id: 242592
ClinVar RCV Id: RCV000515751 RCV000515752
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269801.1:p.Gly355Ser
CA354106
NM_001282872.1:c.1063G>A