Canonical Allele Identifier: PA2828162271
Gene: ADAR HGNC NCBI

Linked Data

ClinVar Variation Id: 39459
ClinVar RCV Id: RCV000032655
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001351975.1:p.Tyr817Phe
CA343779
NM_001365046.1:c.2450A>T