Canonical Allele Identifier: PA2499296774
Gene: SYN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1045598
ClinVar RCV Id: RCV001350039
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_598006.1:p.Gln619Lys
CA412822357
NM_133499.2:c.1855C>A