Canonical Allele Identifier: PA891863588
Gene: ADAR HGNC NCBI

Linked Data

ClinVar Variation Id: 39457
ClinVar RCV Id: RCV000032652
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001102.3:p.Asp1113His
CA343777
NM_001111.5:c.3337G>C