Canonical Allele Identifier: PA1139670666
Gene: CYP11B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 995869
ClinVar RCV Id: RCV001290136 RCV002541804
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001021384.1:p.Val316Met
CA4905245
NM_001026213.1:c.946G>A