Canonical Allele Identifier: PA2828162272
Gene: ADAR HGNC NCBI

Linked Data

ClinVar Variation Id: 39457
ClinVar RCV Id: RCV000032652

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001351975.1:p.Asp818His
CA343777
NM_001365046.1:c.2452G>C