Allele Registry

Canonical Allele Identifier: PA2826778410

Gene: VPS11 HGNC NCBI

ClinVar RCV:

RCV000202610

RCV000203530

RCV001582699

ClinVar Variation:

218366

HGVS (amino-acid)	Matching Registered Transcripts
NP_001277114.1:p.Cys836Gly	CA280077 NM_001290185.2:c.2506T>G