Canonical Allele Identifier: PA2829891186
Gene: VPS13B HGNC NCBI

Linked Data

ClinVar Variation Id: 2180276
ClinVar RCV Id: RCV002602731
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060360.3:p.Lys1024Glu
CA4823141
NM_017890.5:c.3070A>G