Canonical Allele Identifier: PA2828162182
Gene: ADAR HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

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