Canonical Allele Identifier: PA2825318514
Gene: VDR HGNC NCBI

Linked Data

ClinVar Variation Id: 1038600
ClinVar RCV Id: RCV001341929

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001017535.1:p.Ala388Asp
CA384514186
NM_001017535.2:c.1163C>A