Allele Registry

Canonical Allele Identifier: PA096738

Gene: CYP11B2 HGNC NCBI

ClinVar RCV:

RCV001043588

RCV001271159

RCV003463694

ClinVar Variation:

242773

HGVS (amino-acid)	Matching Registered Transcripts
NP_000489.3:p.Arg181Trp	CA038796 NM_000498.3:c.541C>T