Canonical Allele Identifier: PA110635
Gene: CYP27A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 4260
ClinVar RCV Id: RCV000004482 RCV000726759 RCV001252459
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000775.1:p.Arg405Gln
CA340216
NM_000784.4:c.1214G>A