Canonical Allele Identifier: PA658672192
Gene: VPS35 HGNC NCBI

Linked Data

ClinVar Variation Id: 487673
ClinVar RCV Id: RCV000577554
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060676.2:p.Arg524Trp
CA280210644
NM_018206.6:c.1570C>T