Allele Registry

Canonical Allele Identifier: PA1139688280

Gene: ADA HGNC NCBI

ClinVar RCV:

RCV001140807

ClinVar Variation:

897495

HGVS (amino-acid)	Matching Registered Transcripts
NP_001308980.1:p.Arg149Leu	CA409121085 NM_001322051.2:c.446G>T