Allele Registry

Canonical Allele Identifier: PA645405273

Gene: ALG8 HGNC NCBI

ClinVar Allele:

322122

ClinVar RCV:

RCV000283611

RCV002522212

ClinVar Variation:

306227

HGVS (amino-acid)	Matching Registered Transcripts
NP_076984.2:p.Gly11Ala	CA6203607 NM_024079.5:c.32G>C