Allele Registry

Canonical Allele Identifier: PA2828130520

Gene: VDR HGNC NCBI

ClinVar RCV:

RCV000251590

ClinVar Variation:

264696

HGVS (amino-acid)	Matching Registered Transcripts
NP_001351014.1:p.Arg391Ser	CA10588005 NM_001364085.2:c.1171C>A