Allele Registry

Canonical Allele Identifier: PA110767

Gene: CYP27B1 HGNC NCBI

ClinVar RCV:

RCV000001741

ClinVar Variation:

1674

HGVS (amino-acid)	Matching Registered Transcripts
NP_000776.1:p.Glu189Gly	CA115136 NM_000785.4:c.566A>G