Allele Registry

Canonical Allele Identifier: PA110671

Gene: CYP27A1 HGNC NCBI

ClinVar Allele:

19303

ClinVar RCV:

RCV000004485

ClinVar Variation:

4264

HGVS (amino-acid)	Matching Registered Transcripts
NP_000775.1:p.Gly145Glu	CA340219 NM_000784.4:c.434G>A