Canonical Allele Identifier: PA2828161458
Gene: ADAR HGNC NCBI

Linked Data

ClinVar Variation Id: 422292
ClinVar RCV Id: RCV000480726
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001351974.1:p.Arg1010Leu
CA16616993
NM_001365045.1:c.3029_3030delinsTT
CA342635953
NM_001365045.1:c.3029G>T