Canonical Allele Identifier: PA2830317764
Gene: VPS13B HGNC NCBI

Linked Data

ClinVar Variation Id: 2127353
ClinVar RCV Id: RCV003047746
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689777.3:p.Gly3772Ser
CA371792096
NM_152564.5:c.11314G>A