Allele Registry

Canonical Allele Identifier: PA2573177360

Gene: CYP11B1 HGNC NCBI

ClinVar RCV:

RCV002048247

ClinVar Variation:

1514386

HGVS (amino-acid)	Matching Registered Transcripts
NP_001021384.1:p.Pro42Thr	CA372397297 NM_001026213.1:c.124C>A