Canonical Allele Identifier: PA2825283757
Gene: ALG8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1714465
ClinVar RCV Id: RCV002304378
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001007028.1:p.Arg184Ser
CA382117299
NM_001007027.2:c.552G>T
CA382117300
NM_001007027.2:c.552G>C