Allele Registry

Canonical Allele Identifier: PA096669

Gene: CYP11B1 HGNC NCBI

ClinVar RCV:

RCV000001236

ClinVar Variation:

1177

HGVS (amino-acid)	Matching Registered Transcripts
NP_000488.3:p.Asn133His	CA339880 NM_000497.4:c.397A>C