Allele Registry

Canonical Allele Identifier: PA2499232960

Gene: CYP11B1 HGNC NCBI

ClinVar Allele:

1017006

ClinVar RCV:

RCV001332501

RCV003989685

ClinVar Variation:

1030831

HGVS (amino-acid)	Matching Registered Transcripts
NP_000488.3:p.Arg448Pro	CA372391454 NM_000497.4:c.1343G>C