Canonical Allele Identifier: PA916026469
Gene: ADA HGNC NCBI

Linked Data

ClinVar Variation Id: 382795
ClinVar RCV Id: RCV000417424
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001308979.1:p.Ser57Asn
CA16608444
NM_001322050.2:c.170G>A