Allele Registry

Canonical Allele Identifier: PA110839

Gene: CYP27B1 HGNC NCBI

ClinVar RCV:

RCV000001733

ClinVar Variation:

1666

HGVS (amino-acid)	Matching Registered Transcripts
NP_000776.1:p.Thr321Arg	CA115131 NM_000785.4:c.962C>G