Allele Registry

Canonical Allele Identifier: PA252460

Gene: VPS13B HGNC NCBI

ClinVar RCV:

RCV000002961

RCV002512689

ClinVar Variation:

2827

HGVS (amino-acid)	Matching Registered Transcripts
NP_689777.3:p.Ile2795Thr	CA252457 NM_152564.5:c.8384T>C