Canonical Allele Identifier: PA2580524249
Gene: VPS13B HGNC NCBI

Linked Data

ClinVar Variation Id: 2180276
ClinVar RCV Id: RCV002602731
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689777.3:p.Lys1024Glu
CA4823141
NM_152564.5:c.3070A>G