Canonical Allele Identifier: PA1139685893
Gene: VDR HGNC NCBI

Linked Data

ClinVar Variation Id: 882309
ClinVar RCV Id: RCV001111882
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001017536.1:p.Glu445Gln
CA384514100
NM_001017536.2:c.1333G>C