Allele Registry

Canonical Allele Identifier: PA2829907854

Gene: ALG13 HGNC NCBI

ClinVar RCV:

RCV000032994

ClinVar Variation:

39775

HGVS (amino-acid)	Matching Registered Transcripts
NP_060936.1:p.Lys94Glu	CA334441456 NM_018466.6:c.280A>G