Canonical Allele Identifier: PA2580133228
Gene: CYP11B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2075863
ClinVar RCV Id: RCV002978990
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001021384.1:p.Arg282Cys
CA4905281
NM_001026213.1:c.844C>T