Allele Registry

Canonical Allele Identifier: PA645500044

Gene: CYP27B1 HGNC NCBI

ClinVar RCV:

RCV000443114

RCV000723316

ClinVar Variation:

380287

HGVS (amino-acid)	Matching Registered Transcripts
NP_000776.1:p.Gly102Glu	CA16606366 NM_000785.4:c.305G>A