Allele Registry

Canonical Allele Identifier: PA2580405352

Gene: VPS33B HGNC NCBI

ClinVar RCV:

RCV002675529

ClinVar Variation:

1941042

HGVS (amino-acid)	Matching Registered Transcripts
NP_061138.3:p.Gly514Arg	CA7744602 NM_018668.5:c.1540G>C