Canonical Allele Identifier: PA2828162918
Gene: ADAR HGNC NCBI

Linked Data

ClinVar Variation Id: 39458

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001351976.1:p.Gly712Arg
CA130316
NM_001365047.1:c.2134G>A
CA342635918
NM_001365047.1:c.2134G>C