Canonical Allele Identifier: PA2580417153
Gene: VPS13B HGNC NCBI

Linked Data

ClinVar Variation Id: 1713783
ClinVar RCV Id: RCV002295571
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060360.3:p.Gly3812Glu
CA182328697
NM_017890.5:c.11435G>A