Canonical Allele Identifier: PA113756
Gene: ADA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 120299

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269154.1:p.Tyr453Cys
CA150799
NM_001282225.2:c.1358A>G