Canonical Allele Identifier: PA2829850260
Gene: ADAR HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056655.3:p.Tyr1086Phe
CA343779
NM_015840.4:c.3257A>T