Canonical Allele Identifier: PA2827247778
Gene: ALG13 HGNC NCBI

Linked Data

ClinVar Variation Id: 385206
ClinVar RCV Id: RCV000419258

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001311221.1:p.Glu119Gln
CA16608679
NM_001324292.2:c.355G>C