Canonical Allele Identifier: PA2499284050
Gene: VPS13B HGNC NCBI

Linked Data

ClinVar Variation Id: 1012602
ClinVar RCV Id: RCV001310639
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060360.3:p.Met3723Thr
CA371790378
NM_017890.5:c.11168T>C