Canonical Allele Identifier: PA1139703305
Gene: AHR HGNC NCBI

Linked Data

ClinVar Variation Id: 967718
ClinVar RCV Id: RCV001242698
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001612.1:p.Asn663Ser
CA4172215
NM_001621.5:c.1988A>G