Canonical Allele Identifier: PA916026464
Gene: ADA HGNC NCBI

Linked Data

ClinVar Variation Id: 373095

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001308979.1:p.Lys35Glu
CA9871641
NM_001322050.2:c.103A>G