Allele Registry

Canonical Allele Identifier: PA2829907884

Gene: ALG13 HGNC NCBI

ClinVar RCV:

RCV001089751

ClinVar Variation:

870209

HGVS (amino-acid)	Matching Registered Transcripts
NP_060936.1:p.Asn107Ile	CA414248698 NM_018466.6:c.320A>T