Allele Registry

Canonical Allele Identifier: PA102051

Gene: VDR HGNC NCBI

ClinVar RCV:

RCV000008186

ClinVar Variation:

7745

HGVS (amino-acid)	Matching Registered Transcripts
NP_000367.1:p.Gly33Asp	CA119018 NM_000376.3:c.98G>A