Allele Registry

Canonical Allele Identifier: PA645416567

Gene: VPS33B HGNC NCBI

ClinVar RCV:

RCV000253189

RCV000989400

RCV001709550

ClinVar Variation:

261041

HGVS (amino-acid)	Matching Registered Transcripts
NP_061138.3:p.Gly514Ser	CA7744601 NM_018668.5:c.1540G>A