Allele Registry

Canonical Allele Identifier: PA915957349

Gene: CYP11B1 HGNC NCBI

ClinVar Allele:

16213

ClinVar RCV:

RCV000001233

RCV001851528

ClinVar Variation:

1174

HGVS (amino-acid)	Matching Registered Transcripts
NP_001021384.1:p.Arg374Gln	CA339877 NM_001026213.1:c.1121G>A