Canonical Allele Identifier: PA2828130530
Gene: VDR HGNC NCBI

Linked Data

ClinVar Variation Id: 2792281
ClinVar RCV Id: RCV003674992
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001351014.1:p.Ser405Phe
CA384513881
NM_001364085.2:c.1214C>T