Canonical Allele Identifier: PA2573177446
Gene: CYP11B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1516454
ClinVar RCV Id: RCV002026610

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001021384.1:p.Arg384Leu
CA372392511
NM_001026213.1:c.1151G>T