Canonical Allele Identifier: PA916026468
Gene: ADA HGNC NCBI

Linked Data

ClinVar Variation Id: 556213
ClinVar RCV Id: RCV000672186

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001308979.1:p.Glu51Lys
CA409120840
NM_001322050.2:c.151G>A