Allele Registry

Canonical Allele Identifier: PA2825201285

Gene: CYP11B1 HGNC NCBI

ClinVar RCV:

RCV002635044

ClinVar Variation:

1928586

HGVS (amino-acid)	Matching Registered Transcripts
NP_000488.3:p.Arg374Pro	CA372393346 NM_000497.4:c.1121G>C