Canonical Allele Identifier: PA2741819486
Gene: CYP27B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2528376
ClinVar RCV Id: RCV003275203
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000776.1:p.Leu351Gln
CA6658235
NM_000785.4:c.1052T>A