Allele Registry

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Canonical Allele Identifier: PA2830316223

Gene: VPS13B HGNC NCBI

Linked Data

ClinVar Variation Id: 2091761

ClinVar RCV Id: RCV003015767

JSON-LD

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_689777.3:p.Ser2425Arg	CA183041705 NM_152564.5:c.7275C>A CA371875588 NM_152564.5:c.7273A>C CA371875594 NM_152564.5:c.7275C>G