Allele Registry

Canonical Allele Identifier: PA096698

Gene: CYP11B1 HGNC NCBI

ClinVar Allele:

16225

ClinVar RCV:

RCV000001245

RCV000029646

RCV000517938

RCV002490289

ClinVar Variation:

1186

HGVS (amino-acid)	Matching Registered Transcripts
NP_000488.3:p.Pro94Leu	CA213667 NM_000497.4:c.281C>T