Canonical Allele Identifier: PA2580132171
Gene: VDR HGNC NCBI

Linked Data

ClinVar Variation Id: 2429695
ClinVar RCV Id: RCV003127149
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001017536.1:p.Leu413Pro
CA384514474
NM_001017536.2:c.1238T>C