Allele Registry

Canonical Allele Identifier: PA2827247642

Gene: ALG13 HGNC NCBI

ClinVar RCV:

RCV001089751

ClinVar Variation:

870209

HGVS (amino-acid)	Matching Registered Transcripts
NP_001311219.1:p.Asn109Ile	CA414248698 NM_001324290.2:c.326A>T