Allele Registry

Canonical Allele Identifier: PA1139680737

Gene: CYP27B1 HGNC NCBI

ClinVar RCV:

RCV001109504

RCV003313988

ClinVar Variation:

880897

HGVS (amino-acid)	Matching Registered Transcripts
NP_000776.1:p.Arg429His	CA6658161 NM_000785.4:c.1286G>A