Allele Registry

Canonical Allele Identifier: PA110625

Gene: CYP27A1 HGNC NCBI

ClinVar RCV:

RCV000004483

ClinVar Variation:

4261

HGVS (amino-acid)	Matching Registered Transcripts
NP_000775.1:p.Arg395Ser	CA340217 NM_000784.4:c.1183C>A