Allele Registry

Canonical Allele Identifier: PA2825455205

Gene: ALG9 HGNC NCBI

ClinVar RCV:

RCV000003947

ClinVar Variation:

3749

HGVS (amino-acid)	Matching Registered Transcripts
NP_001071160.1:p.Tyr116Cys	CA252862 NM_001077692.2:c.347A>G