Allele Registry

Canonical Allele Identifier: PA2825005138

Gene: ADA HGNC NCBI

ClinVar RCV:

RCV001246793

ClinVar Variation:

971097

HGVS (amino-acid)	Matching Registered Transcripts
NP_000013.2:p.Arg101Gly	CA409121387 NM_000022.3:c.301C>G