Canonical Allele Identifier: PA2825339990
Gene: ADAR HGNC NCBI

Linked Data

ClinVar Variation Id: 422292
ClinVar RCV Id: RCV000480726

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001020278.1:p.Arg706Leu
CA16616993
NM_001025107.3:c.2117_2118delinsTT
CA342635953
NM_001025107.3:c.2117G>T