Canonical Allele Identifier: PA2580405341
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_061138.3:p.Glu456Gly
CA393886489
NM_018668.5:c.1367A>G