Canonical Allele Identifier: PA2827645891
Gene: ALG9 HGNC NCBI

Linked Data

ClinVar Variation Id: 2048922
ClinVar RCV Id: RCV002932129

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339339.1:p.Asn383Ser
CA6274357
NM_001352410.1:c.1148A>G