Canonical Allele Identifier: PA891863541
Gene: ADAR HGNC NCBI

Linked Data

ClinVar Variation Id: 126395

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001102.3:p.Pro193Ala
CA345491
NM_001111.5:c.577C>G