Allele Registry

Canonical Allele Identifier: PA2580133238

Gene: CYP11B1 HGNC NCBI

ClinVar RCV:

RCV002635044

ClinVar Variation:

1928586

HGVS (amino-acid)	Matching Registered Transcripts
NP_001021384.1:p.Arg374Pro	CA372393346 NM_001026213.1:c.1121G>C