Canonical Allele Identifier: PA2825283798
Gene: ALG8 HGNC NCBI

Linked Data

ClinVar Variation Id: 198905

Amino-acid Alleles

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