Canonical Allele Identifier: PA113736
Gene: ADA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 120304
ClinVar Variation Id: 1076271

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269154.1:p.Gly47Arg
CA150810
NM_001282225.2:c.139G>A
CA10088319
NM_001282225.2:c.139G>C