Canonical Allele Identifier: PA2826056413
Gene: ALG13 HGNC NCBI

Linked Data

ClinVar Variation Id: 39775
ClinVar RCV Id: RCV000032994

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001161857.1:p.Lys94Glu
CA334441456
NM_001168385.2:c.280A>G