Allele Registry

Canonical Allele Identifier: PA2826762145

Gene: VPS33B HGNC NCBI

ClinVar RCV:

RCV000253189

RCV000989400

RCV001709550

ClinVar Variation:

261041

HGVS (amino-acid)	Matching Registered Transcripts
NP_001276077.1:p.Gly487Ser	CA7744601 NM_001289148.1:c.1459G>A