Canonical Allele Identifier: PA2826761999
Gene: VPS33B HGNC NCBI

Linked Data

ClinVar Variation Id: 3002945
ClinVar RCV Id: RCV003860536
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001276077.1:p.Ala2Val
CA274765057
NM_001289148.1:c.5C>T