Allele Registry

Canonical Allele Identifier: PA119041

Gene: VDR HGNC NCBI

ClinVar RCV:

RCV000008197

ClinVar Variation:

7756

HGVS (amino-acid)	Matching Registered Transcripts
NP_001017535.1:p.Arg391Cys	CA119040 NM_001017535.2:c.1171C>T