Canonical Allele Identifier: PA2826762298
Gene: VPS33B HGNC NCBI

Linked Data

ClinVar Variation Id: 598185

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001276078.1:p.Asp374Asn
CA7744666
NM_001289149.1:c.1120G>A