Canonical Allele Identifier: PA2825005066
Gene: ADA HGNC NCBI

Linked Data

ClinVar Variation Id: 1523684
ClinVar RCV Id: RCV002039064

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000013.2:p.Glu13Lys
CA409122544
NM_000022.3:c.37G>A