Canonical Allele Identifier: PA148913
Gene: VPS13B HGNC NCBI

Linked Data

ClinVar Variation Id: 95826
ClinVar RCV Id: RCV000081872 RCV000361059 RCV000710109 RCV003964938 RCV002313806
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689777.3:p.Ala3691Thr
CA148910
NM_152564.5:c.11071G>A