Canonical Allele Identifier: PA267232
Gene: VPS35 HGNC NCBI

Linked Data

ClinVar Variation Id: 96727
ClinVar RCV Id: RCV000082874
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060676.2:p.Arg526Cys
CA267231
NM_018206.6:c.1576C>T