Allele Registry

Canonical Allele Identifier: PA2499234155

Gene: CYP27B1 HGNC NCBI

ClinVar RCV:

RCV001378186

ClinVar Variation:

1067033

HGVS (amino-acid)	Matching Registered Transcripts
NP_000776.1:p.Arg453Leu	CA385500827 NM_000785.4:c.1358G>T