Canonical Allele Identifier: PA2580508351
Gene: SYN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2254467
ClinVar RCV Id: RCV002807390
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_598006.1:p.Pro554Ser
CA412822985
NM_133499.2:c.1660C>T