Canonical Allele Identifier: PA2829907899
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_060936.1:p.Glu119Gln
CA16608679
NM_018466.6:c.355G>C