Canonical Allele Identifier: PA2741825470
Gene: VDR HGNC NCBI

Linked Data

ClinVar Variation Id: 2792281
ClinVar RCV Id: RCV003674992

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001017536.1:p.Ser455Phe
CA384513881
NM_001017536.2:c.1364C>T