Canonical Allele Identifier: PA1139742282
Gene: VDR HGNC NCBI

Linked Data

ClinVar Variation Id: 882307

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001351014.1:p.Arg452Gln
CA236505902
NM_001364085.2:c.1355G>A