Canonical Allele Identifier: PA2826762335
Gene: VPS33B HGNC NCBI

Linked Data

ClinVar Variation Id: 499620
ClinVar RCV Id: RCV000591538 RCV000765242
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001276078.1:p.Ser471Asn
CA7744540
NM_001289149.1:c.1412G>A