Allele Registry

Canonical Allele Identifier: PA1139676296

Gene: ALG13 HGNC NCBI

ClinVar RCV:

RCV001089751

ClinVar Variation:

870209

HGVS (amino-acid)	Matching Registered Transcripts
NP_001034299.3:p.Gln87His	CA414248697 NM_001039210.5:c.261A>C CA414248698 NM_001039210.5:c.261A>T