Canonical Allele Identifier: PA2580254749
Gene: AHR HGNC NCBI

Linked Data

ClinVar Variation Id: 1992818
ClinVar RCV Id: RCV002814462

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001612.1:p.Val647Leu
CA366895547
NM_001621.5:c.1939G>C