Allele Registry

Canonical Allele Identifier: PA213483

Gene: ADA HGNC NCBI

ClinVar RCV:

RCV000029302

RCV002513235

ClinVar Variation:

35654

HGVS (amino-acid)	Matching Registered Transcripts
NP_000013.2:p.Ser291Trp	CA085502 NM_000022.3:c.872C>G