Canonical Allele Identifier: PA645418748
Gene: ALG13 HGNC NCBI

Linked Data

ClinVar Variation Id: 423341

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001093392.1:p.Ala81Thr
CA16621181
NM_001099922.3:c.241G>A