Canonical Allele Identifier: PA1139703301
Gene: AHR HGNC NCBI

Linked Data

ClinVar Variation Id: 964083
ClinVar RCV Id: RCV001238230

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001612.1:p.Val630Ala
CA366895426
NM_001621.5:c.1889T>C