Allele Registry

Canonical Allele Identifier: PA2828747674

Gene: VPS11 HGNC NCBI

ClinVar RCV:

RCV000202610

RCV000203530

RCV001582699

ClinVar Variation:

218366

HGVS (amino-acid)	Matching Registered Transcripts
NP_001365147.1:p.Cys850Gly	CA280077 NM_001378218.1:c.2548T>G