Allele Registry

Canonical Allele Identifier: PA252426

Gene: VPS13B HGNC NCBI

ClinVar RCV:

RCV000002953

ClinVar Variation:

2819

HGVS (amino-acid)	Matching Registered Transcripts
NP_689777.3:p.Leu2168Arg	CA252423 NM_152564.5:c.6503T>G