Allele Registry

Canonical Allele Identifier: PA110714

Gene: CYP27B1 HGNC NCBI

ClinVar RCV:

RCV000001739

ClinVar Variation:

1672

HGVS (amino-acid)	Matching Registered Transcripts
NP_000776.1:p.Arg389Gly	CA115134 NM_000785.4:c.1165C>G