Canonical Allele Identifier: PA2742006613
Gene: SYN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2878805
ClinVar RCV Id: RCV003623641
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_598006.1:p.Pro656Ser
CA412822021
NM_133499.2:c.1966C>T