Canonical Allele Identifier: PA2825201325
Gene: CYP11B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1906418
ClinVar RCV Id: RCV002589030
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000488.3:p.Ala399Gly
CA372392160
NM_000497.4:c.1196C>G