Canonical Allele Identifier: PA264021
Gene: VPS13B HGNC NCBI

Linked Data

ClinVar Variation Id: 56641
ClinVar RCV Id: RCV000050054
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689777.3:p.Thr3902_Val3903delinsLys
CA264018
NM_152564.5:c.11705_11709delinsAA