Canonical Allele Identifier: PA1139762294
Gene: VPS13B HGNC NCBI

Linked Data

ClinVar Variation Id: 959569
ClinVar RCV Id: RCV001232947

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689777.3:p.Ser948Thr
CA4823066
NM_152564.5:c.2843G>C