Allele Registry

Canonical Allele Identifier: PA345198

Gene: CYP27A1 HGNC NCBI

ClinVar RCV:

RCV000056112

RCV001268892

RCV003894909

ClinVar Variation:

65867

HGVS (amino-acid)	Matching Registered Transcripts
NP_000775.1:p.Arg137Trp	CA345197 NM_000784.4:c.409C>T