Canonical Allele Identifier: PA2825005209
Gene: ADA HGNC NCBI

Linked Data

ClinVar Variation Id: 1015428
ClinVar RCV Id: RCV001314283

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000013.2:p.Ser192Gly
CA409120799
NM_000022.3:c.574A>G