Allele Registry

Canonical Allele Identifier: PA345170

Gene: CYP27A1 HGNC NCBI

ClinVar Allele:

76746

ClinVar RCV:

RCV000056078

RCV000727395

ClinVar Variation:

65838

HGVS (amino-acid)	Matching Registered Transcripts
NP_000775.1:p.Arg405Trp	CA345169 NM_000784.4:c.1213C>T