Allele Registry

Canonical Allele Identifier: PA916026484

Gene: ADA HGNC NCBI

ClinVar RCV:

RCV000059109

RCV000494092

ClinVar Variation:

68267

HGVS (amino-acid)	Matching Registered Transcripts
NP_001308980.1:p.Gly20Arg	CA266020 NM_001322051.2:c.58G>A CA409122498 NM_001322051.2:c.58G>C