Canonical Allele Identifier: PA2828162080
Gene: ADAR HGNC NCBI

Linked Data

ClinVar Variation Id: 39456
ClinVar RCV Id: RCV000032651

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001351975.1:p.Ala575Thr
CA343775
NM_001365046.1:c.1723G>A