Canonical Allele Identifier: PA2825200862
Gene: CYP11B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2382000
ClinVar RCV Id: RCV002674790
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000488.3:p.His69Gln
CA4905681
NM_000497.4:c.207C>G
CA372397127
NM_000497.4:c.207C>A