Canonical Allele Identifier: PA658830254
Gene: VPS13B HGNC NCBI

Linked Data

ClinVar Variation Id: 551758
ClinVar RCV Id: RCV000666898
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060360.3:p.Ser3964dup
CA658821990
NM_017890.5:c.11889_11891dup