Canonical Allele Identifier: PA2573219650
Gene: AHR HGNC NCBI

Linked Data

ClinVar Variation Id: 1417070
ClinVar RCV Id: RCV001948052

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001612.1:p.Asp598Gly
CA4172183
NM_001621.5:c.1793A>G