Canonical Allele Identifier: PA2828533815
Gene: VDR HGNC NCBI

Linked Data

ClinVar Variation Id: 2444136
ClinVar RCV Id: RCV003152934
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361590.1:p.Arg402Cys
CA384513943
NM_001374661.1:c.1204C>T