Canonical Allele Identifier: PA2829891101
Gene: VPS13B HGNC NCBI

Linked Data

ClinVar Variation Id: 959569
ClinVar RCV Id: RCV001232947

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060360.3:p.Ser948Thr
CA4823066
NM_017890.5:c.2843G>C