Allele Registry

Canonical Allele Identifier: PA2829812205

Gene: VPS13A HGNC NCBI

ClinVar RCV:

RCV000517261

RCV000605550

RCV001580041

ClinVar Variation:

448864

HGVS (amino-acid)	Matching Registered Transcripts
NP_056001.1:p.Tyr1587Cys	CA5092598 NM_015186.4:c.4760A>G