Allele Registry

Canonical Allele Identifier: PA102005

Gene: VDR HGNC NCBI

ClinVar RCV:

RCV000008197

ClinVar Variation:

7756

HGVS (amino-acid)	Matching Registered Transcripts
NP_000367.1:p.Arg391Cys	CA119040 NM_000376.3:c.1171C>T