Canonical Allele Identifier: PA2828164111
Gene: ADAR HGNC NCBI

Linked Data

ClinVar Variation Id: 39461
ClinVar RCV Id: RCV000032657

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001351978.1:p.Ile551Thr
CA343783
NM_001365049.1:c.1652T>C