Canonical Allele Identifier: PA2573270910
Gene: VPS13B HGNC NCBI

Linked Data

ClinVar Variation Id: 1449087
ClinVar RCV Id: RCV002004513

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060360.3:p.Ser2469Thr
CA371875704
NM_017890.5:c.7405T>A