Canonical Allele Identifier: PA2830315667
Gene: VPS13B HGNC NCBI

Linked Data

ClinVar Variation Id: 642509
ClinVar RCV Id: RCV000795987 RCV003955509
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689777.3:p.Ala2016Val
CA4823933
NM_152564.5:c.6047C>T