Canonical Allele Identifier: PA2830317769
Gene: VPS13B HGNC NCBI

Linked Data

ClinVar Variation Id: 2101263
ClinVar RCV Id: RCV003033703
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689777.3:p.Gly3776Glu
CA371792151
NM_152564.5:c.11327G>A