Canonical Allele Identifier: PA2825005220
Gene: ADA HGNC NCBI

Linked Data

ClinVar Variation Id: 967164
ClinVar RCV Id: RCV001242000
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000013.2:p.Gly208Ser
CA9871582
NM_000022.3:c.622G>A