Canonical Allele Identifier: PA645448902
Gene: ADA HGNC NCBI

Linked Data

ClinVar Variation Id: 338506

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000013.2:p.Gly239Ser
CA9871547
NM_000022.3:c.715G>A