Canonical Allele Identifier: PA2826639233
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_001269157.1:p.Trp222Ser
CA150816
NM_001282228.2:c.665G>C