Canonical Allele Identifier: PA2830316879
Gene: VPS13B HGNC NCBI

Linked Data

ClinVar Variation Id: 1422355
ClinVar RCV Id: RCV001926116
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689777.3:p.Asp2878Gly
CA371776067
NM_152564.5:c.8633A>G