Canonical Allele Identifier: PA1139703307
Gene: AHR HGNC NCBI

Linked Data

ClinVar Variation Id: 958185
ClinVar RCV Id: RCV001231302
ClinVar Variation Id: 2097726
ClinVar RCV Id: RCV003028533
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001612.1:p.Asp668Glu
CA366895699
NM_001621.5:c.2004C>A
CA366895700
NM_001621.5:c.2004C>G