Allele Registry

Canonical Allele Identifier: PA2826672126

Gene: RHD HGNC NCBI

ClinVar RCV:

RCV000019286

ClinVar Variation:

17712

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269799.1:p.Leu110Pro	CA127334 NM_001282870.1:c.329T>C