Canonical Allele Identifier: PA2825201298
Gene: CYP11B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2440670
ClinVar RCV Id: RCV003145971
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000488.3:p.Glu383Gly
CA372392526
NM_000497.4:c.1148A>G