Allele Registry

Canonical Allele Identifier: PA2573177369

Gene: CYP11B1 HGNC NCBI

ClinVar RCV:

RCV002019554

ClinVar Variation:

1497921

HGVS (amino-acid)	Matching Registered Transcripts
NP_001021384.1:p.Pro94Gln	CA187466987 NM_001026213.1:c.281C>A