Canonical Allele Identifier: PA2826435642
Gene: ALG13 HGNC NCBI

Linked Data

ClinVar Variation Id: 385206
ClinVar RCV Id: RCV000419258

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244159.1:p.Glu15Gln
CA16608679
NM_001257230.2:c.43G>C