Canonical Allele Identifier: PA2827141942
Gene: ADA HGNC NCBI

Linked Data

ClinVar Variation Id: 1678200
ClinVar RCV Id: RCV002224791 RCV003991047
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001308979.1:p.Asn193Lys
CA9871435
NM_001322050.2:c.579T>A
CA409118668
NM_001322050.2:c.579T>G