Canonical Allele Identifier: PA2827141898
Gene: ADA HGNC NCBI

Linked Data

ClinVar Variation Id: 402341
ClinVar RCV Id: RCV000455891 RCV000780818 RCV000668819
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001308979.1:p.Arg147Gln
CA9871496
NM_001322050.2:c.440G>A