Canonical Allele Identifier: PA2827141918
Gene: ADA HGNC NCBI

Linked Data

ClinVar Variation Id: 897016
ClinVar RCV Id: RCV001140048
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001308979.1:p.Phe165Cys
CA9871470
NM_001322050.2:c.494T>G