Canonical Allele Identifier: PA2580417144
Gene: VPS13B HGNC NCBI

Linked Data

ClinVar Variation Id: 2010946
ClinVar RCV Id: RCV002829124
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060360.3:p.Thr3780Ile
CA371791902
NM_017890.5:c.11339C>T