Canonical Allele Identifier: PA2573176117
Gene: VDR HGNC NCBI

Linked Data

ClinVar Variation Id: 1387284
ClinVar RCV Id: RCV001875527
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001017536.1:p.Asn254His
CA384518537
NM_001017536.2:c.760A>C