Canonical Allele Identifier: PA2830316935
Gene: VPS13B HGNC NCBI

Linked Data

ClinVar Variation Id: 1352697
ClinVar RCV Id: RCV002039888

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689777.3:p.Ser2917Trp
CA371776555
NM_152564.5:c.8750C>G