Allele Registry

Canonical Allele Identifier: PA2826436200

Gene: ALG13 HGNC NCBI

ClinVar Allele:

48374

ClinVar RCV:

RCV000032994

ClinVar Variation:

39775

HGVS (amino-acid)	Matching Registered Transcripts
NP_001244160.1:p.Lys16Glu	CA334441456 NM_001257231.2:c.46A>G