Canonical Allele Identifier: PA915957354
Gene: CYP11B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 550514
ClinVar RCV Id: RCV000665278
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001021384.1:p.Ala386Glu
CA4905092
NM_001026213.1:c.1157C>A