Canonical Allele Identifier: PA1139703294
Gene: AHR HGNC NCBI

Linked Data

ClinVar Variation Id: 859723
ClinVar RCV Id: RCV001065897
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001612.1:p.Tyr599Cys
CA4172184
NM_001621.5:c.1796A>G