Canonical Allele Identifier: PA2828130493
Gene: VDR HGNC NCBI

Linked Data

ClinVar Variation Id: 754732
ClinVar RCV Id: RCV001112345 RCV000932081 RCV003479251
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001351014.1:p.Thr362Ile
CA6533756
NM_001364085.2:c.1085C>T