Canonical Allele Identifier: PA1139670429
Gene: CYP11B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 910245
ClinVar RCV Id: RCV001161920 RCV001163438
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001021384.1:p.Asp82Asn
CA4905579
NM_001026213.1:c.244G>A