Canonical Allele Identifier: PA2573270991
Gene: VPS13B HGNC NCBI

Linked Data

ClinVar Variation Id: 1433938
ClinVar RCV Id: RCV001952760
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060360.3:p.Ser3286Phe
CA371783789
NM_017890.5:c.9857C>T