Canonical Allele Identifier: PA2825283711
Gene: ALG8 HGNC NCBI

Linked Data

ClinVar Variation Id: 2561

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001007028.1:p.Thr47Pro
CA252325
NM_001007027.2:c.139A>C