Allele Registry

Canonical Allele Identifier: PA2827142145

Gene: ADA HGNC NCBI

ClinVar RCV:

RCV000029302

RCV002513235

ClinVar Variation:

35654

HGVS (amino-acid)	Matching Registered Transcripts
NP_001308980.1:p.Ser267Trp	CA085502 NM_001322051.2:c.800C>G