Canonical Allele Identifier: PA2826438035
Gene: ALG13 HGNC NCBI

Linked Data

ClinVar Variation Id: 2438993
ClinVar RCV Id: RCV003141328

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244170.1:p.Leu18Phe
CA414248620
NM_001257241.3:c.52C>T