Canonical Allele Identifier: PA2827141858
Gene: ADA HGNC NCBI

Linked Data

ClinVar Variation Id: 338506

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001308979.1:p.Gly104Ser
CA9871547
NM_001322050.2:c.310G>A