Canonical Allele Identifier: PA2573219669
Gene: AHR HGNC NCBI

Linked Data

ClinVar Variation Id: 1470663
ClinVar RCV Id: RCV001964291
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001612.1:p.Asn673Ser
CA4172220
NM_001621.5:c.2018A>G