Allele Registry

Canonical Allele Identifier: PA1139688010

Gene: ADA HGNC NCBI

ClinVar RCV:

RCV001246793

ClinVar Variation:

971097

HGVS (amino-acid)	Matching Registered Transcripts
NP_001308979.1:p.Cys4Trp	CA409121387 NM_001322050.2:c.12C>G