Canonical Allele Identifier: PA2580132156
Gene: VDR HGNC NCBI

Linked Data

ClinVar Variation Id: 2267460
ClinVar RCV Id: RCV002821543

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001017536.1:p.Leu255Val
CA384518528
NM_001017536.2:c.763C>G