Canonical Allele Identifier: PA2825543629
Gene: ADAR HGNC NCBI

Linked Data

ClinVar Variation Id: 2949974
ClinVar RCV Id: RCV003807332
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001102.3:p.Tyr1222Ser
CA342634439
NM_001111.5:c.3665A>C