Allele Registry

Canonical Allele Identifier: PA2828748588

Gene: VPS11 HGNC NCBI

ClinVar RCV:

RCV000202610

RCV000203530

RCV001582699

ClinVar Variation:

218366

HGVS (amino-acid)	Matching Registered Transcripts
NP_001365150.1:p.Cys840Gly	CA280077 NM_001378221.1:c.2518T>G