Canonical Allele Identifier: PA2830316914
Gene: VPS13B HGNC NCBI

Linked Data

ClinVar Variation Id: 1005055
ClinVar RCV Id: RCV001301859
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689777.3:p.Ile2907Val
CA371776409
NM_152564.5:c.8719A>G