Canonical Allele Identifier: PA913198673
Gene: CYP27A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 597410

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000775.1:p.Thr343Met
CA2112786
NM_000784.4:c.1028C>T