Allele Registry

Canonical Allele Identifier: PA096758

Gene: CYP11B2 HGNC NCBI

ClinVar RCV:

RCV000018375

ClinVar Variation:

16879

HGVS (amino-acid)	Matching Registered Transcripts
NP_000489.3:p.Leu461Pro	CA126943 NM_000498.3:c.1382T>C