Canonical Allele Identifier: PA2573177445
Gene: CYP11B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1487557
ClinVar RCV Id: RCV002033582
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001021384.1:p.Arg384Pro
CA372392508
NM_001026213.1:c.1151G>C