Allele Registry

Canonical Allele Identifier: PA915957300

Gene: CYP11B1 HGNC NCBI

ClinVar RCV:

RCV000001236

ClinVar Variation:

1177

HGVS (amino-acid)	Matching Registered Transcripts
NP_001021384.1:p.Asn133His	CA339880 NM_001026213.1:c.397A>C