Canonical Allele Identifier: PA2580254745
Gene: AHR HGNC NCBI

Linked Data

ClinVar Variation Id: 2157201
ClinVar RCV Id: RCV003077971
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001612.1:p.Val613Ile
CA366895301
NM_001621.5:c.1837G>A