Canonical Allele Identifier: PA2580124354
Gene: CYP11B2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2136711
ClinVar RCV Id: RCV003062184 RCV003459719
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000489.3:p.Ile263Asn
CA372389102
NM_000498.3:c.788T>A