Canonical Allele Identifier: PA1139670673
Gene: CYP11B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 864109
ClinVar RCV Id: RCV001071218
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001021384.1:p.Arg332Gly
CA372394356
NM_001026213.1:c.994C>G