Canonical Allele Identifier: PA2830317936
Gene: VPS13B HGNC NCBI

Linked Data

ClinVar Variation Id: 555004
ClinVar RCV Id: RCV000670738
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689777.3:p.Ser3948del
CA658821991
NM_152564.5:c.11841_11843del