Canonical Allele Identifier: PA2830316944
Gene: VPS13B HGNC NCBI

Linked Data

ClinVar Variation Id: 1055803
ClinVar RCV Id: RCV001364534

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689777.3:p.Gln2919Arg
CA182328759
NM_152564.5:c.8756A>G