Canonical Allele Identifier: PA2826762169
Gene: VPS33B HGNC NCBI

Linked Data

ClinVar Variation Id: 499523
ClinVar RCV Id: RCV000597264
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001276077.1:p.Ser535Ile
CA393884772
NM_001289148.1:c.1604G>T