Canonical Allele Identifier: PA2825005206
Gene: ADA HGNC NCBI

Linked Data

ClinVar Variation Id: 2147602
ClinVar RCV Id: RCV003077270
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000013.2:p.Gly190Glu
CA9871628
NM_000022.3:c.569G>A