Canonical Allele Identifier: PA658664853
Gene: CYP27A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 449362

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000775.1:p.Arg513His
CA2112939
NM_000784.4:c.1538G>A