Canonical Allele Identifier: PA891863586
Gene: ADAR HGNC NCBI

Linked Data

ClinVar Variation Id: 292761

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001102.3:p.His1097Asn
CA1130999
NM_001111.5:c.3289C>A