Canonical Allele Identifier: PA645461434
Gene: CYP11B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 362159
ClinVar RCV Id: RCV000282706 RCV000349385 RCV000875628
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000488.3:p.Tyr275His
CA4905288
NM_000497.4:c.823T>C