Canonical Allele Identifier: PA2830316233
Gene: VPS13B HGNC NCBI

Linked Data

ClinVar Variation Id: 1209715
ClinVar RCV Id: RCV001578972
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689777.3:p.Thr2432Ile
CA371875637
NM_152564.5:c.7295C>T