Allele Registry

Canonical Allele Identifier: PA2826672076

Gene: RHD HGNC NCBI

ClinVar RCV:

RCV000019287

ClinVar Variation:

17713

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269796.1:p.Val104Gly	CA127336 NM_001282867.1:c.311T>G