Canonical Allele Identifier: PA891863587
Gene: ADAR HGNC NCBI

Linked Data

ClinVar Variation Id: 39459
ClinVar RCV Id: RCV000032655

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001102.3:p.Tyr1112Phe
CA343779
NM_001111.5:c.3335A>T