Allele Registry

Canonical Allele Identifier: PA645500183

Gene: CYP27B1 HGNC NCBI

ClinVar RCV:

RCV003226270

RCV003417870

RCV003556305

ClinVar Variation:

267276

HGVS (amino-acid)	Matching Registered Transcripts
NP_000776.1:p.Arg453His	CA6658146 NM_000785.4:c.1358G>A