Canonical Allele Identifier: PA915965251
Gene: CYP27A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 809161
ClinVar RCV Id: RCV000997670 RCV003502583
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000775.1:p.Glu359Gln
CA2112795
NM_000784.4:c.1075G>C