Allele Registry

Canonical Allele Identifier: PA2826056423

Gene: ALG13 HGNC NCBI

ClinVar RCV:

RCV001089751

ClinVar Variation:

870209

HGVS (amino-acid)	Matching Registered Transcripts
NP_001161857.1:p.Asn107Ile	CA414248698 NM_001168385.2:c.320A>T