Canonical Allele Identifier: PA2830317712
Gene: VPS13B HGNC NCBI

Linked Data

ClinVar Variation Id: 655502
ClinVar RCV Id: RCV000811695
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689777.3:p.Arg3716Trp
CA4825153
NM_152564.5:c.11146C>T