Canonical Allele Identifier: PA916012763
Gene: ADA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 120307
ClinVar RCV Id: RCV000106388
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269155.1:p.Trp264Ser
CA150816
NM_001282226.2:c.791G>C