Canonical Allele Identifier: PA2580254751
Gene: AHR HGNC NCBI

Linked Data

ClinVar Variation Id: 2046520
ClinVar RCV Id: RCV002886659
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001612.1:p.Cys664Tyr
CA366895667
NM_001621.5:c.1991G>A