Canonical Allele Identifier: PA2827141931
Gene: ADA HGNC NCBI

Linked Data

ClinVar Variation Id: 1195941
ClinVar RCV Id: RCV001559239
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001308979.1:p.Arg178Trp
CA9871463
NM_001322050.2:c.532C>T