Allele Registry

Canonical Allele Identifier: PA2573268398

Gene: RHD HGNC NCBI

ClinVar Allele:

32751

ClinVar RCV:

RCV000019286

ClinVar Variation:

17712

HGVS (amino-acid)	Matching Registered Transcripts
NP_057208.3:p.Leu110Pro	CA127334 NM_016124.6:c.329T>C