Canonical Allele Identifier: PA916026474
Gene: ADA HGNC NCBI

Linked Data

ClinVar Variation Id: 1957

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001308979.1:p.Arg76His
CA252000
NM_001322050.2:c.227G>A