Canonical Allele Identifier: PA2741826188
Gene: CYP11B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2674660
ClinVar RCV Id: RCV003459904
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001021384.1:p.Leu340Arg
CA4905179
NM_001026213.1:c.1019T>G