Canonical Allele Identifier: PA915957351
Gene: CYP11B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 557468
ClinVar RCV Id: RCV000673616

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001021384.1:p.Leu382Arg
CA372392543
NM_001026213.1:c.1145T>G