Canonical Allele Identifier: PA2826762241
Gene: VPS33B HGNC NCBI

Linked Data

ClinVar Variation Id: 317425
ClinVar RCV Id: RCV000293071 RCV002520979
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001276078.1:p.Arg199Trp
CA7744879
NM_001289149.1:c.595C>T