Allele Registry

Canonical Allele Identifier: PA204879

Gene: VPS35 HGNC NCBI

ClinVar RCV:

RCV000190799

ClinVar Variation:

208774

HGVS (amino-acid)	Matching Registered Transcripts
NP_060676.2:p.Gln488Arg	CA204878 NM_018206.6:c.1463A>G