Canonical Allele Identifier: PA096677
Gene: CYP11B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 948654

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000488.3:p.Gly379Val
CA372392611
NM_000497.4:c.1136G>T