Canonical Allele Identifier: PA2828163043
Gene: ADAR HGNC NCBI

Linked Data

ClinVar Variation Id: 14820
ClinVar RCV Id: RCV000015943

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001351976.1:p.Phe870Ser
CA124351
NM_001365047.1:c.2609T>C