Canonical Allele Identifier: PA113089
Gene: ALG8 HGNC NCBI

Linked Data

ClinVar Variation Id: 2561

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_076984.2:p.Thr47Pro
CA252325
NM_024079.5:c.139A>C