Canonical Allele Identifier: PA2829892381
Gene: VPS13B HGNC NCBI

Linked Data

ClinVar Variation Id: 3188767
ClinVar RCV Id: RCV004482662

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060360.3:p.Ala3720Gly
CA371790343
NM_017890.5:c.11159C>G