Allele Registry

Canonical Allele Identifier: PA2825283798

Gene: ALG8 HGNC NCBI

ClinVar Allele:

196065

ClinVar RCV:

RCV000180366

RCV000590852

ClinVar Variation:

198905

HGVS (amino-acid)	Matching Registered Transcripts
NP_001007028.1:p.Trp286Gly	CA247803 NM_001007027.2:c.856T>G