Canonical Allele Identifier: PA1139730358
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_060360.3:p.Thr2451Ser
CA371875597
NM_017890.5:c.7351A>T
CA371875599
NM_017890.5:c.7352C>G