Canonical Allele Identifier: PA2580549159
Gene: VPS13B HGNC NCBI

Linked Data

ClinVar Variation Id: 2086154
ClinVar RCV Id: RCV002996554
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_858047.2:p.Pro8Ala
CA371856021
NM_181661.3:c.22C>G