Allele Registry

Canonical Allele Identifier: PA916026482

Gene: ADA HGNC NCBI

ClinVar RCV:

RCV000059102

RCV000429669

ClinVar Variation:

68263

HGVS (amino-acid)	Matching Registered Transcripts
NP_001308980.1:p.His15Asp	CA266012 NM_001322051.2:c.43C>G