Canonical Allele Identifier: PA916044618
Gene: VDR HGNC NCBI

Linked Data

ClinVar Variation Id: 308873
ClinVar RCV Id: RCV000300530
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001351014.1:p.Arg452Trp
CA10632865
NM_001364085.2:c.1354C>T