Allele Registry

Canonical Allele Identifier: PA915957303

Gene: CYP11B1 HGNC NCBI

ClinVar RCV:

RCV000029647

RCV001158699

RCV001165427

RCV003565385

ClinVar Variation:

35989

HGVS (amino-acid)	Matching Registered Transcripts
NP_001021384.1:p.Arg138His	CA213668 NM_001026213.1:c.413G>A