Canonical Allele Identifier: PA2826762127
Gene: VPS33B HGNC NCBI

Linked Data

ClinVar Variation Id: 2479408
ClinVar RCV Id: RCV003204184
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001276077.1:p.Glu429Gly
CA393886489
NM_001289148.1:c.1286A>G