Canonical Allele Identifier: PA2830317942
Gene: VPS13B HGNC NCBI

Linked Data

ClinVar Variation Id: 2093660
ClinVar RCV Id: RCV002996849
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689777.3:p.Cys3953Tyr
CA371795777
NM_152564.5:c.11858G>A