Allele Registry

Canonical Allele Identifier: PA110736

Gene: CYP27B1 HGNC NCBI

ClinVar RCV:

RCV000255484

RCV001329404

RCV003987480

ClinVar Variation:

265095

HGVS (amino-acid)	Matching Registered Transcripts
NP_000776.1:p.Arg429Pro	CA10588555 NM_000785.4:c.1286G>C