Canonical Allele Identifier: PA2499298914
Gene: VPS13B HGNC NCBI

Linked Data

ClinVar Variation Id: 1009282
ClinVar RCV Id: RCV001306747
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689777.3:p.Ser999Pro
CA371865699
NM_152564.5:c.2995T>C