Allele Registry

Canonical Allele Identifier: PA2827142091

Gene: ADA HGNC NCBI

ClinVar RCV:

RCV000538818

RCV003403304

ClinVar Variation:

468281

HGVS (amino-acid)	Matching Registered Transcripts
NP_001308980.1:p.Arg211Trp	CA9871550 NM_001322051.2:c.631C>T