Canonical Allele Identifier: PA2825005148
Gene: ADA HGNC NCBI

Linked Data

ClinVar Variation Id: 1046026
ClinVar RCV Id: RCV001350532
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000013.2:p.Trp117Arg
CA9871702
NM_000022.3:c.349T>C
CA409121295
NM_000022.3:c.349T>A