Canonical Allele Identifier: PA2580124372
Gene: CYP11B2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2335488
ClinVar RCV Id: RCV002954522
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000489.3:p.Val316Met
CA4906033
NM_000498.3:c.946G>A