Allele Registry

Canonical Allele Identifier: PA096770

Gene: CYP11B2 HGNC NCBI

ClinVar RCV:

RCV000018377

RCV000808165

RCV001826477

RCV002496398

ClinVar Variation:

16881

HGVS (amino-acid)	Matching Registered Transcripts
NP_000489.3:p.Thr185Ile	CA126946 NM_000498.3:c.554C>T