Allele Registry

Canonical Allele Identifier: PA180491

Gene: VPS13B HGNC NCBI

ClinVar Allele:

177257

ClinVar RCV:

RCV000154132

RCV000871803

RCV002316976

RCV003430714

ClinVar Variation:

167835

HGVS (amino-acid)	Matching Registered Transcripts
NP_689777.3:p.Asn3351Ile	CA180488 NM_152564.5:c.10052A>T