Canonical Allele Identifier: PA2826187462
Gene: ADAR HGNC NCBI

Linked Data

ClinVar Variation Id: 39460
ClinVar RCV Id: RCV000032656

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001180424.1:p.Lys704Asn
CA343781
NM_001193495.2:c.2112G>T
CA342635965
NM_001193495.2:c.2112G>C