Allele Registry

Canonical Allele Identifier: PA916026460

Gene: ADA HGNC NCBI

ClinVar RCV:

RCV000059098

ClinVar Variation:

68259

HGVS (amino-acid)	Matching Registered Transcripts
NP_001308979.1:p.Gly5Cys	CA266003 NM_001322050.2:c.13G>T