Allele Registry

Canonical Allele Identifier: PA915957289

Gene: CYP11B1 HGNC NCBI

ClinVar RCV:

RCV000001245

RCV000029646

RCV000517938

RCV002490289

ClinVar Variation:

1186

HGVS (amino-acid)	Matching Registered Transcripts
NP_001021384.1:p.Pro94Leu	CA213667 NM_001026213.1:c.281C>T