Canonical Allele Identifier: PA2825339986
Gene: ADAR HGNC NCBI

Linked Data

ClinVar Variation Id: 39460
ClinVar RCV Id: RCV000032656

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001020278.1:p.Lys704Asn
CA343781
NM_001025107.3:c.2112G>T
CA342635965
NM_001025107.3:c.2112G>C