Canonical Allele Identifier: PA2573159744
Gene: ADA HGNC NCBI

Linked Data

ClinVar Variation Id: 1352394
ClinVar RCV Id: RCV002047570
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000013.2:p.Met315Thr
CA9871459
NM_000022.3:c.944T>C