Canonical Allele Identifier: PA2825201231
Gene: CYP11B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2195750
ClinVar RCV Id: RCV002628917
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000488.3:p.Arg332Trp
CA4905184
NM_000497.4:c.994C>T