Canonical Allele Identifier: PA2742006603
Gene: SYN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2772180
ClinVar RCV Id: RCV003510938
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_598006.1:p.Arg622Trp
CA412822323
NM_133499.2:c.1864C>T