Canonical Allele Identifier: PA2828162339
Gene: ADAR HGNC NCBI

Linked Data

ClinVar Variation Id: 2202842
ClinVar RCV Id: RCV002664179
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001351975.1:p.Tyr897Asp
CA342634663
NM_001365046.1:c.2689T>G