Allele Registry

Canonical Allele Identifier: PA119037

Gene: VDR HGNC NCBI

ClinVar RCV:

RCV000008195

ClinVar Variation:

7754

HGVS (amino-acid)	Matching Registered Transcripts
NP_001017535.1:p.His305Gln	CA119036 NM_001017535.2:c.915C>G CA384515929 NM_001017535.2:c.915C>A