Allele Registry

Canonical Allele Identifier: PA915956589

Gene: VDR HGNC NCBI

ClinVar RCV:

RCV000251590

ClinVar Variation:

264696

HGVS (amino-acid)	Matching Registered Transcripts
NP_001017536.1:p.Arg441Ser	CA10588005 NM_001017536.2:c.1321C>A