Allele Registry

Canonical Allele Identifier: PA110790

Gene: CYP27B1 HGNC NCBI

ClinVar RCV:

RCV000001726

ClinVar Variation:

1659

HGVS (amino-acid)	Matching Registered Transcripts
NP_000776.1:p.Gly125Glu	CA115125 NM_000785.4:c.374G>A