Allele Registry

Canonical Allele Identifier: PA2825653637

Gene: RHD HGNC NCBI

ClinVar RCV:

RCV000019286

ClinVar Variation:

17712

HGVS (amino-acid)	Matching Registered Transcripts
NP_001121163.1:p.Leu110Pro	CA127334 NM_001127691.3:c.329T>C