Canonical Allele Identifier: PA2573173677
Gene: CYP27A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1372342
ClinVar RCV Id: RCV001872912

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000775.1:p.Asp354Asn
CA350591573
NM_000784.4:c.1060G>A