Canonical Allele Identifier: PA1139688119
Gene: ADA HGNC NCBI

Linked Data

ClinVar Variation Id: 967164
ClinVar RCV Id: RCV001242000
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001308979.1:p.Gly73Ser
CA9871582
NM_001322050.2:c.217G>A