Canonical Allele Identifier: PA2825201226
Gene: CYP11B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 864109
ClinVar RCV Id: RCV001071218

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000488.3:p.Arg332Gly
CA372394356
NM_000497.4:c.994C>G