Allele Registry

Canonical Allele Identifier: PA102027

Gene: VDR HGNC NCBI

ClinVar RCV:

RCV000008187

RCV000522189

ClinVar Variation:

7746

HGVS (amino-acid)	Matching Registered Transcripts
NP_000367.1:p.Arg73Gln	CA119020 NM_000376.3:c.218G>A