Canonical Allele Identifier: PA916045027
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_001351977.1:p.Asp818His
CA343777
NM_001365048.1:c.2452G>C