Canonical Allele Identifier: PA645416546
Gene: VPS33B HGNC NCBI

Linked Data

ClinVar Variation Id: 317423
ClinVar RCV Id: RCV000372554 RCV000729557 RCV000899084 RCV001252830 RCV003940242
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_061138.3:p.Ile383Thr
CA7744773
NM_018668.5:c.1148T>C