Canonical Allele Identifier: PA2830317696
Gene: VPS13B HGNC NCBI

Linked Data

ClinVar Variation Id: 860557
ClinVar RCV Id: RCV001066882
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689777.3:p.Arg3700Trp
CA4825143
NM_152564.5:c.11098C>T