Canonical Allele Identifier: PA2825382916
Gene: ALG13 HGNC NCBI

Linked Data

ClinVar Variation Id: 385206
ClinVar RCV Id: RCV000419258
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001034299.3:p.Arg99Thr
CA16608679
NM_001039210.5:c.296G>C