Canonical Allele Identifier: PA658827322
Gene: CYP11B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 552238

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000488.3:p.Arg384Gln
CA4905094
NM_000497.4:c.1151G>A