Canonical Allele Identifier: PA252460
Gene: VPS13B HGNC NCBI

Linked Data

ClinVar Variation Id: 2827

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689777.3:p.Ile2795Thr
CA252457
NM_152564.5:c.8384T>C