Allele Registry

Canonical Allele Identifier: PA110803

Gene: CYP27B1 HGNC NCBI

ClinVar Allele:

16712

ClinVar RCV:

RCV000001740

ClinVar Variation:

1673

HGVS (amino-acid)	Matching Registered Transcripts
NP_000776.1:p.Leu343Phe	CA115135 NM_000785.4:c.1027C>T