Allele Registry

Canonical Allele Identifier: PA2825502637

Gene: ALG13 HGNC NCBI

ClinVar RCV:

RCV001089751

ClinVar Variation:

870209

HGVS (amino-acid)	Matching Registered Transcripts
NP_001093392.1:p.Asn107Ile	CA414248698 NM_001099922.3:c.320A>T