Allele Registry

Canonical Allele Identifier: PA3057455308

Gene: CYP11B1 HGNC NCBI

ClinVar Allele:

3725967

ClinVar RCV:

RCV005040983

ClinVar Variation:

3595315

HGVS (amino-acid)	Matching Registered Transcripts
NP_001021384.1:p.Ser315Arg	CA372395052 NM_001026213.1:c.945C>G CA372395053 NM_001026213.1:c.945C>A CA372395065 NM_001026213.1:c.943A>C