Allele Registry

Canonical Allele Identifier: PA110694

Gene: CYP27B1 HGNC NCBI

ClinVar RCV:

RCV000001727

ClinVar Variation:

1660

HGVS (amino-acid)	Matching Registered Transcripts
NP_000776.1:p.Arg335Pro	CA115126 NM_000785.4:c.1004G>C