Canonical Allele Identifier: PA2826762339
Gene: VPS33B HGNC NCBI

Linked Data

ClinVar Variation Id: 286121
ClinVar RCV Id: RCV000331023 RCV003967750 RCV003987492
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001276078.1:p.Phe481Val
CA7744533
NM_001289149.1:c.1441T>G