Allele Registry

Canonical Allele Identifier: PA110725

Gene: CYP27B1 HGNC NCBI

ClinVar RCV:

RCV000001736

RCV000481523

RCV001195099

ClinVar Variation:

1669

HGVS (amino-acid)	Matching Registered Transcripts
NP_000776.1:p.Arg389His	CA115133 NM_000785.4:c.1166G>A