Canonical Allele Identifier: PA2580213108
Gene: ADA HGNC NCBI

Linked Data

ClinVar Variation Id: 2105223
ClinVar RCV Id: RCV003023344

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001308980.1:p.Thr26Pro
CA409122462
NM_001322051.2:c.76A>C