Allele Registry

Canonical Allele Identifier: PA2827645792

Gene: ALG9 HGNC NCBI

ClinVar RCV:

RCV000274374

RCV001850600

ClinVar Variation:

302425

HGVS (amino-acid)	Matching Registered Transcripts
NP_001339338.1:p.Arg376Trp	CA6274361 NM_001352409.1:c.1126C>T