Canonical Allele Identifier: PA2499284071
Gene: VPS13B HGNC NCBI

Linked Data

ClinVar Variation Id: 1008752
ClinVar RCV Id: RCV001306142
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060360.3:p.Thr2459Ile
CA371875647
NM_017890.5:c.7376C>T