Canonical Allele Identifier: PA2830317759
Gene: VPS13B HGNC NCBI

Linked Data

ClinVar Variation Id: 1052994
ClinVar RCV Id: RCV001361276
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689777.3:p.Val3769Ile
CA371792066
NM_152564.5:c.11305G>A