Canonical Allele Identifier: PA2828162813
Gene: ADAR HGNC NCBI

Linked Data

ClinVar Variation Id: 39461
ClinVar RCV Id: RCV000032657
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001351976.1:p.Ile577Thr
CA343783
NM_001365047.1:c.1730T>C