Canonical Allele Identifier: PA2573270964
Gene: VPS13B HGNC NCBI

Linked Data

ClinVar Variation Id: 1352697
ClinVar RCV Id: RCV002039888
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060360.3:p.Ser2942Trp
CA371776555
NM_017890.5:c.8825C>G