Canonical Allele Identifier: PA2829681578
Gene: SYN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2050831
ClinVar RCV Id: RCV002904645
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008881.2:p.Gln585Arg
CA412822687
NM_006950.3:c.1754A>G