Canonical Allele Identifier: PA916026485
Gene: ADA HGNC NCBI

Linked Data

ClinVar Variation Id: 570007
ClinVar RCV Id: RCV000690764 RCV001507463
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001308980.1:p.Ser21Ala
CA9871785
NM_001322051.2:c.61T>G