Allele Registry

Canonical Allele Identifier: PA2827142056

Gene: ADA HGNC NCBI

ClinVar RCV:

RCV000059107

ClinVar Variation:

68265

HGVS (amino-acid)	Matching Registered Transcripts
NP_001308980.1:p.Val177Met	CA266016 NM_001322051.2:c.529G>A