Canonical Allele Identifier: PA916026507
Gene: ADA HGNC NCBI

Linked Data

ClinVar Variation Id: 1979

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001308980.1:p.Leu152Met
CA115292
NM_001322051.2:c.454C>A