Allele Registry

Canonical Allele Identifier: PA2825200825

Gene: CYP11B1 HGNC NCBI

ClinVar RCV:

RCV002048247

ClinVar Variation:

1514386

HGVS (amino-acid)	Matching Registered Transcripts
NP_000488.3:p.Pro42Thr	CA372397297 NM_000497.4:c.124C>A