Canonical Allele Identifier: PA2830317749
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_689777.3:p.Thr3755Ile
CA371791902
NM_152564.5:c.11264C>T