Canonical Allele Identifier: PA916060101
Gene: VPS13B HGNC NCBI

Linked Data

ClinVar Variation Id: 655502
ClinVar RCV Id: RCV000811695

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060360.3:p.Arg3741Trp
CA4825153
NM_017890.5:c.11221C>T