Allele Registry

Canonical Allele Identifier: PA213669

Gene: CYP11B1 HGNC NCBI

ClinVar RCV:

RCV000029647

RCV001158699

RCV001165427

RCV003565385

ClinVar Variation:

35989

HGVS (amino-acid)	Matching Registered Transcripts
NP_000488.3:p.Arg138His	CA213668 NM_000497.4:c.413G>A