Canonical Allele Identifier: PA645405127
Gene: SYN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 436901
ClinVar RCV Id: RCV000501441 RCV001857173 RCV002383974
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_598006.1:p.Ala441Thr
CA10398367
NM_133499.2:c.1321G>A