Allele Registry

Canonical Allele Identifier: PA2827142097

Gene: ADA HGNC NCBI

ClinVar RCV:

RCV000378500

RCV003230481

ClinVar Variation:

338506

HGVS (amino-acid)	Matching Registered Transcripts
NP_001308980.1:p.Gly215Ser	CA9871547 NM_001322051.2:c.643G>A