Canonical Allele Identifier: PA916026467
Gene: ADA HGNC NCBI

Linked Data

ClinVar Variation Id: 68266
ClinVar RCV Id: RCV000059108
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001308979.1:p.Ala44Asp
CA266018
NM_001322050.2:c.131C>A