Allele Registry

Canonical Allele Identifier: PA102063

Gene: VDR HGNC NCBI

ClinVar RCV:

RCV000008194

ClinVar Variation:

7753

HGVS (amino-acid)	Matching Registered Transcripts
NP_000367.1:p.Gly46Asp	CA119034 NM_000376.3:c.137G>A