Allele Registry

Canonical Allele Identifier: PA2827646117

Gene: ALG9 HGNC NCBI

ClinVar Allele:

18788

ClinVar RCV:

RCV000003947

ClinVar Variation:

3749

HGVS (amino-acid)	Matching Registered Transcripts
NP_001339342.1:p.Tyr116Cys	CA252862 NM_001352413.1:c.347A>G