Canonical Allele Identifier: PA2830317742
Gene: VPS13B HGNC NCBI

Linked Data

ClinVar Variation Id: 1720684
ClinVar RCV Id: RCV002305201
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689777.3:p.Ile3744Val
CA371791745
NM_152564.5:c.11230A>G