Canonical Allele Identifier: PA645448886
Gene: ADA HGNC NCBI

Linked Data

ClinVar Variation Id: 338509
ClinVar RCV Id: RCV000377525 RCV001375517
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000013.2:p.His197Gln
CA9871621
NM_000022.3:c.591T>A
CA409120766
NM_000022.3:c.591T>G