Allele Registry

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Canonical Allele Identifier: PA2830316902

Gene: VPS13B HGNC NCBI

Linked Data

ClinVar Variation Id: 1346725

ClinVar RCV Id: RCV002030161

JSON-LD

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_689777.3:p.His2899Gln	CA371776323 NM_152564.5:c.8697C>G CA371776325 NM_152564.5:c.8697C>A