Canonical Allele Identifier: PA2580254746
Gene: AHR HGNC NCBI

Linked Data

ClinVar Variation Id: 2123935
ClinVar RCV Id: RCV003035664

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001612.1:p.Gln614Pro
CA366895310
NM_001621.5:c.1841A>C