Canonical Allele Identifier: PA2829907856
Gene: ALG13 HGNC NCBI

Linked Data

ClinVar Variation Id: 1303764

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060936.1:p.Pro95Leu
CA414248617
NM_018466.6:c.284C>T