Canonical Allele Identifier: PA2825283697
Gene: ALG8 HGNC NCBI

Linked Data

ClinVar Variation Id: 306227

Amino-acid Alleles

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