Allele Registry

Canonical Allele Identifier: PA110703

Gene: CYP27B1 HGNC NCBI

ClinVar RCV:

RCV001868859

ClinVar Variation:

1324206

HGVS (amino-acid)	Matching Registered Transcripts
NP_000776.1:p.Arg389Cys	CA6658200 NM_000785.4:c.1165C>T