Canonical Allele Identifier: PA2826762103
Gene: VPS33B HGNC NCBI

Linked Data

ClinVar Variation Id: 317423
ClinVar RCV Id: RCV000372554 RCV000729557 RCV000899084 RCV001252830 RCV003940242
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001276077.1:p.Ile356Thr
CA7744773
NM_001289148.1:c.1067T>C