Allele Registry

Canonical Allele Identifier: PA645463629

Gene: VPS13A HGNC NCBI

ClinVar Variation Id: 367407

HGVS (amino-acid)	Matching Registered Transcripts
NP_150648.2:p.Glu2360Lys	CA5093209 NM_033305.3:c.7078G>A