Canonical Allele Identifier: PA2829851930
Gene: ADAR HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056656.3:p.Tyr1067Phe
CA343779
NM_015841.4:c.3200A>T