Canonical Allele Identifier: PA2829907854
Gene: ALG13 HGNC NCBI

Linked Data

ClinVar Variation Id: 39775
ClinVar RCV Id: RCV000032994
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060936.1:p.Lys94Glu
CA334441456
NM_018466.6:c.280A>G