Canonical Allele Identifier: PA2827142079
Gene: ADA HGNC NCBI

Linked Data

ClinVar Variation Id: 2050660
ClinVar RCV Id: RCV002904551
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001308980.1:p.Gln199Arg
CA409120756
NM_001322051.2:c.596A>G