Canonical Allele Identifier: PA891863538
Gene: ADAR HGNC NCBI

Linked Data

ClinVar Variation Id: 500335
ClinVar Variation Id: 1373677
ClinVar RCV Id: RCV001877433

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001102.3:p.Arg100Gly
CA1131722
NM_001111.5:c.298A>G
CA2573131084
NM_001111.5:c.297_298delinsTG