Canonical Allele Identifier: PA2830317950
Gene: VPS13B HGNC NCBI

Linked Data

ClinVar Variation Id: 1462307
ClinVar RCV Id: RCV001985661
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689777.3:p.Glu3959Val
CA371795853
NM_152564.5:c.11876A>T