Canonical Allele Identifier: PA2741826183
Gene: CYP11B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2674658
ClinVar RCV Id: RCV003459902
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001021384.1:p.Gly267Asp
CA372395356
NM_001026213.1:c.800G>A