Canonical Allele Identifier: PA2741886590
Gene: AHR HGNC NCBI

Linked Data

ClinVar Variation Id: 2526605
ClinVar RCV Id: RCV004300838
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001612.1:p.Phe572Leu
CA366895026
NM_001621.5:c.1714T>C
CA366895031
NM_001621.5:c.1716C>A
CA366895032
NM_001621.5:c.1716C>G