Canonical Allele Identifier: PA2828162818
Gene: ADAR HGNC NCBI

Linked Data

ClinVar Variation Id: 1396756
ClinVar RCV Id: RCV001887490
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001351976.1:p.Ser583Pro
CA342636817
NM_001365047.1:c.1747T>C