Canonical Allele Identifier: PA2826672141
Gene: RHD HGNC NCBI

Linked Data

ClinVar Variation Id: 17713
ClinVar RCV Id: RCV000019287

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269799.1:p.Val270Gly
CA127336
NM_001282870.1:c.809T>G