Canonical Allele Identifier: PA2828533995
Gene: VDR HGNC NCBI

Linked Data

ClinVar Variation Id: 308878

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361591.1:p.Ala350Thr
CA6533769
NM_001374662.1:c.1048G>A