Allele Registry

Canonical Allele Identifier: PA2829811671

Gene: VPS13A HGNC NCBI

ClinVar RCV:

RCV000347795

RCV000518783

RCV001562536

RCV002523807

ClinVar Variation:

367364

HGVS (amino-acid)	Matching Registered Transcripts
NP_056001.1:p.Ser734Asn	CA5091890 NM_015186.4:c.2201G>A