Allele Registry

Canonical Allele Identifier: PA213655

Gene: CYP11B1 HGNC NCBI

ClinVar RCV:

RCV000029638

RCV002250464

RCV002496449

ClinVar Variation:

35982

HGVS (amino-acid)	Matching Registered Transcripts
NP_000488.3:p.Arg374Trp	CA213654 NM_000497.4:c.1120C>T