Canonical Allele Identifier: PA2580117437
Gene: CYP27B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2180339
ClinVar RCV Id: RCV002602768 RCV003250786
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000776.1:p.Arg104Trp
CA6658501
NM_000785.4:c.310C>T