Canonical Allele Identifier: PA2830317706
Gene: VPS13B HGNC NCBI

Linked Data

ClinVar Variation Id: 1981686
ClinVar RCV Id: RCV002751610
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689777.3:p.Glu3712Lys
CA371790569
NM_152564.5:c.11134G>A