Canonical Allele Identifier: PA2825339887
Gene: ADAR HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001020278.1:p.Ala575Thr
CA343775
NM_001025107.3:c.1723G>A