Allele Registry

Canonical Allele Identifier: PA2825283697

Gene: ALG8 HGNC NCBI

ClinVar Allele:

322122

ClinVar RCV:

RCV000283611

RCV002522212

ClinVar Variation:

306227

HGVS (amino-acid)	Matching Registered Transcripts
NP_001007028.1:p.Gly11Ala	CA6203607 NM_001007027.2:c.32G>C