Canonical Allele Identifier: PA2499258631
Gene: AHR HGNC NCBI

Linked Data

ClinVar Variation Id: 1124242

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001612.1:p.Val660Met
CA4172212
NM_001621.5:c.1978G>A