Canonical Allele Identifier: PA2827141913
Gene: ADA HGNC NCBI

Linked Data

ClinVar Variation Id: 1505857
ClinVar RCV Id: RCV002004261
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001308979.1:p.Pro162Leu
CA9871472
NM_001322050.2:c.485C>T