Allele Registry

Canonical Allele Identifier: PA096748

Gene: CYP11B2 HGNC NCBI

ClinVar RCV:

RCV000793582

RCV001271158

RCV001535987

RCV003549354

ClinVar Variation:

242702

2697591

HGVS (amino-acid)	Matching Registered Transcripts
NP_000489.3:p.Glu198Asp	CA038911 NM_000498.3:c.594A>C CA372390288 NM_000498.3:c.594A>T