Canonical Allele Identifier: PA2580124370
Gene: CYP11B2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1697321
ClinVar RCV Id: RCV002267703 RCV003560905 RCV003464423
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000489.3:p.Ser308Pro
CA372388477
NM_000498.3:c.922T>C