Allele Registry

Canonical Allele Identifier: PA2826762146

Gene: VPS33B HGNC NCBI

ClinVar RCV:

RCV002675529

ClinVar Variation:

1941042

HGVS (amino-acid)	Matching Registered Transcripts
NP_001276077.1:p.Gly487Arg	CA7744602 NM_001289148.1:c.1459G>C