Canonical Allele Identifier: PA2830312578
Gene: VPS13B HGNC NCBI

Linked Data

ClinVar Variation Id: 2086154
ClinVar RCV Id: RCV002996554
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689777.3:p.Pro8Ala
CA371856021
NM_152564.5:c.22C>G