Canonical Allele Identifier: PA2829819642
Gene: VPS13B HGNC NCBI

Linked Data

ClinVar Variation Id: 2086154
ClinVar RCV Id: RCV002996554

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056058.2:p.Pro8Ala
CA371856021
NM_015243.3:c.22C>G