Allele Registry

Canonical Allele Identifier: PA2825160013

Gene: VDR HGNC NCBI

ClinVar RCV:

RCV000421461

ClinVar Variation:

381603

HGVS (amino-acid)	Matching Registered Transcripts
NP_000367.1:p.Arg343Cys	CA16606541 NM_000376.3:c.1027C>T