Allele Registry

Canonical Allele Identifier: PA2573268403

Gene: RHD HGNC NCBI

ClinVar RCV:

RCV000019287

ClinVar Variation:

17713

HGVS (amino-acid)	Matching Registered Transcripts
NP_057208.3:p.Val270Gly	CA127336 NM_016124.6:c.809T>G