Allele Registry

Canonical Allele Identifier: PA102287

Gene: VPS13B HGNC NCBI

ClinVar RCV:

RCV000002958

ClinVar Variation:

2824

HGVS (amino-acid)	Matching Registered Transcripts
NP_060360.3:p.Gly2645Asp	CA252443 NM_017890.5:c.7934G>A