Allele Registry

Canonical Allele Identifier: PA2825200820

Gene: CYP11B1 HGNC NCBI

ClinVar RCV:

RCV002033028

ClinVar Variation:

1347207

HGVS (amino-acid)	Matching Registered Transcripts
NP_000488.3:p.Pro42Ala	CA372397298 NM_000497.4:c.124C>G