Canonical Allele Identifier: PA2828162912
Gene: ADAR HGNC NCBI

Linked Data

ClinVar Variation Id: 422292
ClinVar RCV Id: RCV000480726

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001351976.1:p.Arg706Leu
CA16616993
NM_001365047.1:c.2117_2118delinsTT
CA342635953
NM_001365047.1:c.2117G>T