Allele Registry

Canonical Allele Identifier: PA096782

Gene: CYP11B2 HGNC NCBI

ClinVar RCV:

RCV000018381

RCV003460485

ClinVar Variation:

16885

HGVS (amino-acid)	Matching Registered Transcripts
NP_000489.3:p.Thr498Ala	CA126948 NM_000498.3:c.1492A>G