Allele Registry

Canonical Allele Identifier: PA3057315233

Gene: CYP27B1 HGNC NCBI

ClinVar RCV:

RCV004703019

ClinVar Variation:

3339277

HGVS (amino-acid)	Matching Registered Transcripts
NP_000776.1:p.Gly125Val	CA385507593 NM_000785.4:c.374G>T