Allele Registry

Canonical Allele Identifier: PA2826438039

Gene: ALG13 HGNC NCBI

ClinVar RCV:

RCV001089751

ClinVar Variation:

870209

HGVS (amino-acid)	Matching Registered Transcripts
NP_001244170.1:p.Asn29Ile	CA414248698 NM_001257241.3:c.86A>T