Allele Registry

Canonical Allele Identifier: PA2826672119

Gene: RHD HGNC NCBI

ClinVar RCV:

RCV000019287

ClinVar Variation:

17713

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269798.1:p.Val270Gly	CA127336 NM_001282869.2:c.809T>G