Allele Registry

Canonical Allele Identifier: PA1139670666

Gene: CYP11B1 HGNC NCBI

ClinVar Allele:

983570

ClinVar RCV:

RCV001290136

RCV002541804

ClinVar Variation:

995869

HGVS (amino-acid)	Matching Registered Transcripts
NP_001021384.1:p.Val316Met	CA4905245 NM_001026213.1:c.946G>A