Canonical Allele Identifier: PA1139668460
Gene: ADA HGNC NCBI

Linked Data

ClinVar Variation Id: 897016
ClinVar RCV Id: RCV001140048
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000013.2:p.Phe300Cys
CA9871470
NM_000022.3:c.899T>G