Allele Registry

Canonical Allele Identifier: PA252446

Gene: VPS13B HGNC NCBI

ClinVar RCV:

RCV000002958

ClinVar Variation:

2824

HGVS (amino-acid)	Matching Registered Transcripts
NP_689777.3:p.Gly2620Asp	CA252443 NM_152564.5:c.7859G>A