Canonical Allele Identifier: PA2829851739
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_056656.3:p.Lys954Asn
CA343781
NM_015841.4:c.2862G>T
CA342635965
NM_015841.4:c.2862G>C