Canonical Allele Identifier: PA2826762295
Gene: VPS33B HGNC NCBI

Linked Data

ClinVar Variation Id: 2479408
ClinVar RCV Id: RCV003204184

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001276078.1:p.Glu365Gly
CA393886489
NM_001289149.1:c.1094A>G