Canonical Allele Identifier: PA2829681617
Gene: SYN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2087362
ClinVar RCV Id: RCV003009521
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008881.2:p.Thr649Ile
CA412822076
NM_006950.3:c.1946C>T