Canonical Allele Identifier: PA2580132173
Gene: VDR HGNC NCBI

Linked Data

ClinVar Variation Id: 2137319
ClinVar RCV Id: RCV003062490
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001017536.1:p.Arg441His
CA6533730
NM_001017536.2:c.1322G>A