Allele Registry

Canonical Allele Identifier: PA119039

Gene: VDR HGNC NCBI

ClinVar RCV:

RCV000008196

RCV002512896

ClinVar Variation:

7755

HGVS (amino-acid)	Matching Registered Transcripts
NP_001017535.1:p.Ile314Ser	CA119038 NM_001017535.2:c.941T>G