Canonical Allele Identifier: PA2825201152
Gene: CYP11B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2674658
ClinVar RCV Id: RCV003459902
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000488.3:p.Gly267Asp
CA372395356
NM_000497.4:c.800G>A