Canonical Allele Identifier: PA2828130502
Gene: VDR HGNC NCBI

Linked Data

ClinVar Variation Id: 2519398
ClinVar RCV Id: RCV003265413
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001351014.1:p.Arg370Gly
CA6533747
NM_001364085.2:c.1108C>G