Allele Registry

Canonical Allele Identifier: PA091225

Gene: ADA HGNC NCBI

ClinVar Allele:

16997

ClinVar RCV:

RCV000002035

ClinVar Variation:

1958

HGVS (amino-acid)	Matching Registered Transcripts
NP_000013.2:p.Leu304Arg	CA252002 NM_000022.3:c.911T>G