Canonical Allele Identifier: PA2829850260
Gene: ADAR HGNC NCBI

Linked Data

ClinVar Variation Id: 39459
ClinVar RCV Id: RCV000032655
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056655.3:p.Tyr1086Phe
CA343779
NM_015840.4:c.3257A>T