Canonical Allele Identifier: PA2825160031
Gene: VDR HGNC NCBI

Linked Data

ClinVar Variation Id: 2192776
ClinVar RCV Id: RCV002643821

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000367.1:p.Asn361Ser
CA6533757
NM_000376.3:c.1082A>G