Canonical Allele Identifier: PA2825339901
Gene: ADAR HGNC NCBI

Linked Data

ClinVar Variation Id: 2049013

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001020278.1:p.Val589Ile
CA1131206
NM_001025107.3:c.1765G>A