Canonical Allele Identifier: PA2825340075
Gene: ADAR HGNC NCBI

Linked Data

ClinVar Variation Id: 39459
ClinVar RCV Id: RCV000032655

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001020278.1:p.Tyr817Phe
CA343779
NM_001025107.3:c.2450A>T