Canonical Allele Identifier: PA223415
Gene: VPS13B HGNC NCBI

Linked Data

ClinVar Variation Id: 95842

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060360.3:p.Ile949Met
CA223412
NM_017890.5:c.2847A>G