Allele Registry

Canonical Allele Identifier: PA2827141913

Gene: ADA HGNC NCBI

ClinVar RCV:

RCV002004261

ClinVar Variation:

1505857

HGVS (amino-acid)	Matching Registered Transcripts
NP_001308979.1:p.Pro162Leu	CA9871472 NM_001322050.2:c.485C>T