Allele Registry

Canonical Allele Identifier: PA096687

Gene: CYP11B1 HGNC NCBI

ClinVar RCV:

RCV000001238

RCV000029642

RCV001851529

RCV002476907

ClinVar Variation:

1179

HGVS (amino-acid)	Matching Registered Transcripts
NP_000488.3:p.Pro42Ser	CA213660 NM_000497.4:c.124C>T