Canonical Allele Identifier: PA2829891141
Gene: VPS13B HGNC NCBI

Linked Data

ClinVar Variation Id: 2194700
ClinVar RCV Id: RCV002647486
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060360.3:p.Val984Leu
CA4823123
NM_017890.5:c.2950G>C