Canonical Allele Identifier: PA2828534013
Gene: VDR HGNC NCBI

Linked Data

ClinVar Variation Id: 2519398
ClinVar RCV Id: RCV003265413

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361591.1:p.Arg370Gly
CA6533747
NM_001374662.1:c.1108C>G