Allele Registry

Canonical Allele Identifier: PA213662

Gene: CYP11B1 HGNC NCBI

ClinVar RCV:

RCV000029643

RCV001852593

RCV002482915

RCV003460492

ClinVar Variation:

35986

HGVS (amino-acid)	Matching Registered Transcripts
NP_000488.3:p.Pro42Leu	CA213661 NM_000497.4:c.125C>T