Canonical Allele Identifier: PA2825159932
Gene: VDR HGNC NCBI

Linked Data

ClinVar Variation Id: 2267460
ClinVar RCV Id: RCV002821543
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000367.1:p.Leu205Val
CA384518528
NM_000376.3:c.613C>G