Canonical Allele Identifier: PA2825005207
Gene: ADA HGNC NCBI

Linked Data

ClinVar Variation Id: 960745
ClinVar RCV Id: RCV001234325
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000013.2:p.Ser191Asn
CA409120803
NM_000022.3:c.572G>A