Canonical Allele Identifier: PA2580133242
Gene: CYP11B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1906418
ClinVar RCV Id: RCV002589030

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001021384.1:p.Ala399Gly
CA372392160
NM_001026213.1:c.1196C>G