Canonical Allele Identifier: PA2828162182
Gene: ADAR HGNC NCBI

Linked Data

ClinVar Variation Id: 39460
ClinVar RCV Id: RCV000032656
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001351975.1:p.Lys704Asn
CA343781
NM_001365046.1:c.2112G>T
CA342635965
NM_001365046.1:c.2112G>C