Canonical Allele Identifier: PA2580132169
Gene: VDR HGNC NCBI

Linked Data

ClinVar Variation Id: 1926137
ClinVar RCV Id: RCV002626259
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001017536.1:p.Arg408Cys
CA6533759
NM_001017536.2:c.1222C>T