Canonical Allele Identifier: PA2827142073
Gene: ADA HGNC NCBI

Linked Data

ClinVar Variation Id: 1015428
ClinVar RCV Id: RCV001314283
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001308980.1:p.Ser192Gly
CA409120799
NM_001322051.2:c.574A>G