Canonical Allele Identifier: PA2580133240
Gene: CYP11B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2440670
ClinVar RCV Id: RCV003145971

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001021384.1:p.Glu383Gly
CA372392526
NM_001026213.1:c.1148A>G