Canonical Allele Identifier: PA891854746
Gene: VPS13B HGNC NCBI

Linked Data

ClinVar Variation Id: 588073

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060360.3:p.Ser2446Cys
CA183041702
NM_017890.5:c.7337C>G