Canonical Allele Identifier: PA658827323
Gene: CYP11B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 550514
ClinVar RCV Id: RCV000665278

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000488.3:p.Ala386Glu
CA4905092
NM_000497.4:c.1157C>A