Allele Registry

Canonical Allele Identifier: PA062268

Gene: VPS11 HGNC NCBI

ClinVar RCV:

RCV000202610

RCV000203530

RCV001582699

ClinVar Variation:

218366

HGVS (amino-acid)	Matching Registered Transcripts
NP_068375.3:p.Cys846Gly	CA280077 NM_021729.6:c.2536T>G