Canonical Allele Identifier: PA658827305
Gene: CYP11B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 553208
ClinVar RCV Id: RCV000668604 RCV001161915 RCV001868223
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000488.3:p.Trp116Gly
CA4905551
NM_000497.4:c.346T>G