Canonical Allele Identifier: PA645461435
Gene: CYP11B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 424028
ClinVar RCV Id: RCV000484244 RCV002481537
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000488.3:p.Ala279Thr
CA4905285
NM_000497.4:c.835G>A