Allele Registry

Canonical Allele Identifier: PA645405317

Gene: ALG8 HGNC NCBI

ClinVar Variation Id: 306226

HGVS (amino-acid)	Matching Registered Transcripts
NP_076984.2:p.Tyr84Cys	CA6203545 NM_024079.5:c.251A>G