Canonical Allele Identifier: PA1139688103
Gene: ADA HGNC NCBI

Linked Data

ClinVar Variation Id: 960745
ClinVar RCV Id: RCV001234325
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001308979.1:p.Ser56Asn
CA409120803
NM_001322050.2:c.167G>A