Allele Registry

Canonical Allele Identifier: PA2573093320

Gene: VPS13B HGNC NCBI

ClinVar Variation Id: 1338320

HGVS (amino-acid)	Matching Registered Transcripts
NP_060360.3:p.Glu2935Lys	CA4824532 NM_017890.5:c.8803G>A