Allele Registry

Canonical Allele Identifier: PA096639

Gene: CYP11B1 HGNC NCBI

ClinVar RCV:

RCV000001233

RCV001851528

ClinVar Variation:

1174

HGVS (amino-acid)	Matching Registered Transcripts
NP_000488.3:p.Arg374Gln	CA339877 NM_000497.4:c.1121G>A