Allele Registry

Canonical Allele Identifier: PA2829812430

Gene: VPS13A HGNC NCBI

ClinVar RCV:

RCV000310297

RCV000710282

RCV001729570

RCV003912583

ClinVar Variation:

367395

HGVS (amino-acid)	Matching Registered Transcripts
NP_056001.1:p.Arg1962Cys	CA5092885 NM_015186.4:c.5884C>T