Allele Registry

Canonical Allele Identifier: PA2825200900

Gene: CYP11B1 HGNC NCBI

ClinVar RCV:

RCV002019554

ClinVar Variation:

1497921

HGVS (amino-acid)	Matching Registered Transcripts
NP_000488.3:p.Pro94Gln	CA187466987 NM_000497.4:c.281C>A