Canonical Allele Identifier: PA110746
Gene: CYP27B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 802871
ClinVar RCV Id: RCV000988872 RCV002479154
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000776.1:p.Arg453Cys
CA6658147
NM_000785.4:c.1357C>T