Allele Registry

Canonical Allele Identifier: PA2826437971

Gene: ALG13 HGNC NCBI

ClinVar RCV:

RCV001089751

ClinVar Variation:

870209

HGVS (amino-acid)	Matching Registered Transcripts
NP_001244168.1:p.Asn3Ile	CA414248698 NM_001257239.1:c.8A>T