Canonical Allele Identifier: PA891863580
Gene: ADAR HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001102.3:p.Lys999Asn
CA343781
NM_001111.5:c.2997G>T
CA342635965
NM_001111.5:c.2997G>C