Allele Registry

Canonical Allele Identifier: PA915957281

Gene: CYP11B1 HGNC NCBI

ClinVar RCV:

RCV000029643

RCV001852593

RCV002482915

RCV003460492

ClinVar Variation:

35986

HGVS (amino-acid)	Matching Registered Transcripts
NP_001021384.1:p.Pro42Leu	CA213661 NM_001026213.1:c.125C>T