Canonical Allele Identifier: PA891863582
Gene: ADAR HGNC NCBI

Linked Data

ClinVar Variation Id: 39458
ClinVar RCV Id: RCV000032653 RCV000032654 RCV000762850 RCV001091722
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001102.3:p.Gly1007Arg
CA130316
NM_001111.5:c.3019G>A
CA342635918
NM_001111.5:c.3019G>C