Canonical Allele Identifier: PA891863569
Gene: ADAR HGNC NCBI

Linked Data

ClinVar Variation Id: 292774

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001102.3:p.Val616Ile
CA1131444
NM_001111.5:c.1846G>A