Canonical Allele Identifier: PA645485011
Gene: CYP11B2 HGNC NCBI

Linked Data

ClinVar Variation Id: 362229
ClinVar RCV Id: RCV000268061 RCV000320888 RCV000377865 RCV001271162 RCV000969225
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000489.3:p.Arg30Gln
CA4906376
NM_000498.3:c.89G>A