Canonical Allele Identifier: PA2829851593
Gene: ADAR HGNC NCBI

Linked Data

ClinVar Variation Id: 39461
ClinVar RCV Id: RCV000032657

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056656.3:p.Ile827Thr
CA343783
NM_015841.4:c.2480T>C