Canonical Allele Identifier: PA150805
Gene: ADA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 120301

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269156.1:p.Gly5Ala
CA150803
NM_001282227.2:c.14G>C