Canonical Allele Identifier: PA2826187367
Gene: ADAR HGNC NCBI

Linked Data

ClinVar Variation Id: 1373686
ClinVar RCV Id: RCV001877437
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001180424.1:p.Ile578Thr
CA342636852
NM_001193495.2:c.1733T>C