Allele Registry

Canonical Allele Identifier: PA645485310

Gene: CYP11B2 HGNC NCBI

ClinVar RCV:

RCV000393406

RCV000455482

RCV001162097

RCV001162098

RCV001271149

RCV001511981

RCV002140371

ClinVar Variation:

362192

1641842

HGVS (amino-acid)	Matching Registered Transcripts
NP_000489.3:p.Gly435Ser	CA4905846 NM_000498.3:c.1303G>A CA2573142868 NM_000498.3:c.1302_1303delinsTA