Canonical Allele Identifier: PA2826762075
Gene: VPS33B HGNC NCBI

Linked Data

ClinVar Variation Id: 317425
ClinVar RCV Id: RCV000293071 RCV002520979
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001276077.1:p.Arg263Trp
CA7744879
NM_001289148.1:c.787C>T