Canonical Allele Identifier: PA916060102
Gene: VPS13B HGNC NCBI

Linked Data

ClinVar Variation Id: 657513
ClinVar RCV Id: RCV000814125 RCV002433968 RCV003396428
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060360.3:p.Glu3749Lys
CA4825158
NM_017890.5:c.11245G>A