Canonical Allele Identifier: PA2499258632
Gene: AHR HGNC NCBI

Linked Data

ClinVar Variation Id: 1015449
ClinVar RCV Id: RCV001314311 RCV004034310
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001612.1:p.Val674Ile
CA4172221
NM_001621.5:c.2020G>A