Canonical Allele Identifier: PA916026476
Gene: ADA HGNC NCBI

Linked Data

ClinVar Variation Id: 1967

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001308979.1:p.Ala80Thr
CA115287
NM_001322050.2:c.238G>A