Canonical Allele Identifier: PA2828130489
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_001351014.1:p.Arg358Cys
CA6533759
NM_001364085.2:c.1072C>T