Allele Registry

Canonical Allele Identifier: PA102298

Gene: VPS13B HGNC NCBI

ClinVar RCV:

RCV000002961

RCV002512689

ClinVar Variation:

2827

HGVS (amino-acid)	Matching Registered Transcripts
NP_060360.3:p.Ile2820Thr	CA252457 NM_017890.5:c.8459T>C