Canonical Allele Identifier: PA2828533776
Gene: VDR HGNC NCBI

Linked Data

ClinVar Variation Id: 1926137
ClinVar RCV Id: RCV002626259

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361590.1:p.Arg358Cys
CA6533759
NM_001374661.1:c.1072C>T