Allele Registry

Canonical Allele Identifier: PA2825382902

Gene: ALG13 HGNC NCBI

ClinVar RCV:

RCV000032994

ClinVar Variation:

39775

HGVS (amino-acid)	Matching Registered Transcripts
NP_001034299.3:p.Lys74Arg	CA334441456 NM_001039210.5:c.221A>G