Canonical Allele Identifier: PA2828130404
Gene: VDR HGNC NCBI

Linked Data

ClinVar Variation Id: 1387284
ClinVar RCV Id: RCV001875527

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001351014.1:p.Asn204His
CA384518537
NM_001364085.2:c.610A>C