Canonical Allele Identifier: PA2830316225
Gene: VPS13B HGNC NCBI

Linked Data

ClinVar Variation Id: 844070
ClinVar RCV Id: RCV001046831
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689777.3:p.Thr2426Ser
CA371875597
NM_152564.5:c.7276A>T
CA371875599
NM_152564.5:c.7277C>G