Allele Registry

Canonical Allele Identifier: PA110812

Gene: CYP27B1 HGNC NCBI

ClinVar RCV:

RCV000001728

RCV001851560

ClinVar Variation:

1661

HGVS (amino-acid)	Matching Registered Transcripts
NP_000776.1:p.Pro382Ser	CA115127 NM_000785.4:c.1144C>T