Canonical Allele Identifier: PA916044620
Gene: VDR HGNC NCBI

Linked Data

ClinVar Variation Id: 308870
ClinVar RCV Id: RCV000278062 RCV002285307 RCV003920281
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001351014.1:p.Phe490Val
CA10632861
NM_001364085.2:c.1468T>G