Canonical Allele Identifier: PA891854804
Gene: VPS13B HGNC NCBI

Linked Data

ClinVar Variation Id: 574541
ClinVar RCV Id: RCV000696497
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060360.3:p.Asp2903Val
CA371776069
NM_017890.5:c.8708A>T