Canonical Allele Identifier: PA2827142074
Gene: ADA HGNC NCBI

Linked Data

ClinVar Variation Id: 382795
ClinVar RCV Id: RCV000417424

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001308980.1:p.Ser192Asn
CA16608444
NM_001322051.2:c.575G>A